38
Inspections
66
Deficiencies
1
Actual Harm or Above
65
Occurrences
July 21, 2026
Last Inspection
S/S D/E/F Potential for harmS/S G Actual harm
The most recent inspection of PELICAN POINTE HEALTH AND REHABILITATION CENTER on record is dated July 21, 2026. Across 38 published inspections, state surveyors cited 66 deficiencies, 1 of which reached actual harm or immediate jeopardy.
Colorado publishes inspections on a rolling window, so older surveys may no longer appear. Citation codes 0000 and 9999 are the surveyor's opening and closing comments, not deficiencies, and are excluded from the counts above. Where the state required one, the facility's own plan of correction is shown beneath the finding it answers.
Provider Information
Status
Active
Facility Type
SNF/NF Dual Certification
Administrator
Hribar, Kenneth Asovalu
Owner
BELMONT RIDGE HEALTHCARE, INC.
Phone
(970) 686-7474
Payor Source
Medicare, Medicaid, Private Pay
City
WINDSOR
ZIP
80550-5484
Inspections & Citations
38 inspections · 66 deficiencies7/21/2026Complaint Survey · ID 2AA81A-H11 deficiency▼
0000INITIAL COMMENTSSurveyor note▼
Findings
A complaint survey, prompted by #CO3048303 and #CO3105308 was conducted on 7/21/26. One deficiency was cited.
Plan of correction
The state did not require a plan of correction for this citation.
0609Reporting of Alleged Violations▼
Findings
Based on record review and interviews, the facility failed to report alleged violations of sexual abuse to the State Survey and Certification Agency in accordance with state law for two (#3 and #4) of two residents reviewed for abuse out of four sample residents. Specifically, the facility failed to ensure an incident of alleged sexual abuse between Resident #4 and Resident #3 was reported to the State Survey Agency. Findings include:Record review and interviews confirmed the facility corrected the deficient practice prior to the onsite investigation on 7/21/26, resulting in the deficiency being cited as past noncompliance with a correction date of 6/15/26. I. Incident of sexual abuse on 6/6/26 On 6/6/26 a certified nurse aide (CNA) reported Resident #4 was restless all night, constantly getting up and trying to wake up her roommate, Resident #3. The CNA placed a chair outside the residents’ room with the door open, so when Resident #4 got up she could lay her back in bed. After assisting another resident down the hall, the CNA returned to the chair. When she returned to the chair outside the residents’ room, she heard Resident #3 saying “What are you doing?” The CNA entered the residents’ room and saw Resident #4 sitting on the edge of her Resident #3’s bed with her hand inside the brief of Resident #3. The CNA asked Resident #4 to return to her bed.-However, the facility failed to report the allegation of sexual abuse to the State Agency. II. Facility plan of correctionA. Immediate action to correct the deficient practice The corrective action plan the facility implemented in response to the sexual abuse incident involving Resident #4 and Resident #3 on 6/6/26 was received from the nursing home administrator (NHA) on 7/21/26 at 9:00 a.m. The corrective action plan revealed that upon notification of the sexual abuse allegation involving Resident #4 and Resident #3 that occurred on 6/6/26, the facility immediately separated both residents. Resident #4 was moved to a different room. Resident #3 was assessed by a nurse and no signs or symptoms of trauma or injury were noted. Resident #3 remained at her mood and behavior baseline and had no evidence of physical or emotional injury. On 6/6/26, the NHA initiated an investigation that included 17 residents residing on the secured unit. Based on the staff and sample residents’ interviews, the NHA unsubstantiated the allegation of sexual abuse. The facility policy and procedure requires that all allegations of abuse will be reported immediately to the appropriate state agency. On 6/10/26 the facility medical director reviewed the records of alleged sexual abuse between Resident #4 and Resident #3 and documented that there appeared to be no medical issue that needed to be worked up at this time. Staff had followed up appropriately and would continue to monitor. On 6/11/26, as Resident #3’s representative was packing the resident’s belongings for a planned transfer to another facility, a CNA informed her of the incident that occured with Resident #4 on the night of 6/6/26. The representative took Resident #3 to an emergency department (ED) at a local hospital for an evaluation. Resident #3’s ED medical record revealed no vaginal injuries and the resident was discharged with a course of antibiotics for a urinary tract infection (UTI). The facility reported the alleged sexual abuse incident to the State Agency on 6/12/26 at 5:00 p.m. On 6/15/26, the NHA received one-on-one re-education on abuse investigations and reporting to the State Agency by a corporate operations manager. III. Facility policy and procedure The Reporting Alleged Violations of Abuse, Neglect, Exploitation or Mistreatment, revised December 2023, was provided by the NHA on 7/21/26 at 4:01 p.m. It read in pertinent part, “If there is an allegation or suspicion of abuse, the facility will make a report to the appropriate agencies as designated by State and Federal laws. In response to allegations of abuse, neglect, exploitation, or mistreatment, the facility will ensure that all alleged violations involving abuse, neglect, exploitations or mistreatment, including injuries of unknown source and misappropriation of resident property, are reported immediately but not later than two (2) hours after the allegation is made if the events that cause the allegation involves abuse or results in serious bodily injury.”IV. Resident #3 (victim)A. Resident statusResident #3, age 85, was admitted on 10/18/21 and discharged on 6/11/26. According to the June 2026 computerized physician orders (CPO), diagnoses included dementia with other behavioral disturbance, anxiety disorder, personal history of transient ischemic attack (TIA) and cerebral infarction without residual deficits, and cognitive communication deficit. The 5/11/26 minimum data set (MDS) assessment revealed the resident had severe cognitive impairment with a brief interview for mental status (BIMS) score of three out of 15. She was dependent on staff assistance with toileting hygiene and bathing, required substantial assistance with all transfers, and used a wheelchair for mobility. The assessment indicated the resident had wandering behavior present on four to six days during the assessment look-back period. B. Record reviewResident #3’s behavior care plan, initiated 9/9/24, revealed she demonstrated physical behaviors towards others, she was verbally aggressive, tearful, and voiced anxiety and distress at times. She had a history of seeing young children urinating on her bed. Interventions included analyzing key times, places, circumstances, triggers, and what de-escalated the resident’s behavior and documenting, Assessing and anticipating the resident's needs, such as food, thirst, toileting needs, comfort level, body positioning and pain.-Review of Resident #3’s electronic medical record (EMR) revealed no progress notes regarding the incident with Resident #4 on 6/6/26. V. Resident #4 (assailant)A. Resident statusResident #4, age 72, was admitted on 10/2/25 and re-admitted on 2/26/26. According to the June 2026 CPO, diagnoses included Alzheimer's disease, unspecified dementia, unspecified severity, with other behavioral disturbance, anxiety disorder and bipolar disorder. The 4/2/26 MDS assessment revealed the resident had severe cognitive impairment with a BIMS score of four out of 15. She required substantial assistance with toileting hygiene, moderate assistance with bathing, transfers and walking with supervision. The assessment indicated the resident had wandering behavior daily during the assessment look-back period. B. Record reviewResident #4’s behavior care plan, initiated 10/16/25, revealed she demonstrated physical & verbal behaviors towards staff, and wandered aimlessly into other residents' rooms. Interventions included, "chores" like sweeping, washing dishes, or folding, non-alcoholic margarita mix and sweets, allow her to call her daughter or husband on the phone, sound machine in room, take for walks, allow resident to sleep in as long as desired, and redirect her when she is encroaching on the personal space of peers. On 6/6/26 a social worker documented she met with Resident #4 about an alleged incident with another resident (Resident #3). Resident #4 was in the common area with other residents listening to music. Resident #4 did not recall the alleged incident. She was observed interacting with staff and peers as per her usual routine and was displaying no signs of psychosocial or physical distress. V. Staff interviewsThe NHA was interviewed on 7/21/26 at 8:45 a.m. The NHA said he immediately initiated an investigation of the incident on 6/6/26 involving Resident #3 and Resident #4 after it was reported to him. He said the investigation included interviews with all interviewable residents in the female memory care unit. The NHA said the investigation identified there were no concerns from others about Resident #4’s inappropriate behavior. He said Resident #4 worked in a healthcare profession prior to her retirement. He said the CNA who reported the incident could not explain if she observed Resident #4 touching Resident #3 inappropriately in her bikini area or if she was just touching the undergarment/brief. The NHA said the facility completed a physical and emotional assessment on both residents immediately and identified no harm or injury to either resident, therefore he did not substantiate the allegation of sexual abuse and did not report the allegation to the State Agency. The NHA was interviewed again on 7/21/26 at 2:30 p.m. The NHA said after he learned the Resident #3’s representative took the resident to the ED for evaluation related to sexual abuse, he contacted his clinical resource. He said on 6/12/26 the facility initiated re-education with all facility staff members that included abuse identification, prevention and reporting. The NHA said all residents on the secured units were interviewed and family members were contacted. He said the facility initiated a plan of correction for abuse and reporting. He said the interdisciplinary team (IDT) initiated reviewing the facility's 24-hour report for any behavior or abuse concerns for all facility residents. He said the plan of correction, the Abuse Reporting policy and the facility’s grievance process had been reviewed in the QAPI meeting on 6/15/26. The NHA said Resident #4 was transferred to another nursing facility per her family’s choice. Registered nurse (RN) #1 was interviewed on 7/21/26 at 12:49 p.m. RN #1 said she knew Resident #4 and Resident #3 very well. She said both residents wandered around the unit and occasionally encroached on other residents’ personal space, which led to verbal disputes. She said Resident #4 exhibited attachment to some staff by hugging them. She said she had not observed any inappropriate sexual behaviors for either of the residents. CNA #1 was interviewed on 7/21/26 at 1:00 p.m. CNA #1 said she worked 12-hour day shifts and knew both Resident #4 and Resident #3. She said Resident #4 was a “very lovely lady” who was always around the staff and in the dining room, participating in activities. She said Resident #4 liked to hug staff, but there were no incidents of her being inappropriate.
Plan of correction
The state did not require a plan of correction for this citation.
7/21/2026Licensure Complaint Survey · ID 2AA81B-H1No deficiencies▼
0000Initial CommentsSurveyor note▼
Findings
A survey with #CO3048304 was completed on 7/21/26. No deficiencies were cited.
Plan of correction
The state did not require a plan of correction for this citation.
7/14/2026Revisit: Complaint Survey · ID 232887-H2No deficiencies▼
0000INITIAL COMMENTSSurveyor note▼
Findings
A revisit survey was completed on 7/14/26 for all previous deficiencies cited on 5/19/26. The facility is in compliance with all regulations surveyed.
Plan of correction
The state did not require a plan of correction for this citation.
7/14/2026Revisit: Licensure Complaint Survey · ID 232889-H2No deficiencies▼
0000Initial CommentsSurveyor note▼
Findings
A revisit survey was completed on 7/14/26 for all previous deficiencies cited on 5/19/26. The facility is in compliance with all regulations surveyed.
Plan of correction
The state did not require a plan of correction for this citation.
7/8/2026Revisit: Recertification Survey · ID 1E05DD-L2No deficiencies▼
9999FINAL OBSERVATIONSSurveyor note▼
Findings
Based on the facility's stated plan for maintaining facility safety, The Centers for Medicare and Medicaid Services granted a "continuous" waiver for use of evaporative coolers for K521 due to the financial hardship that would be imposed in moving to a different mechanism for facility cooling.
Plan of correction
The state did not require a plan of correction for this citation.
5/19/2026Complaint Survey · ID 232887-H13 deficiencies▼
0000INITIAL COMMENTSSurveyor note▼
Findings
A complaint survey, prompted by #CO2995141, #CO2995387, #CO3013464 and Incident #3006286 was completed on 5/18/26 to 5/19/26. Three deficiencies were cited.
Plan of correction
The state did not require a plan of correction for this citation.
0684Quality of Care▼
Findings
Based on record review and interviews, the facility failed to provide treatment and care in accordance with professional standards for one (#5) of six residents out of nine sample residents. Specifically, the facility failed to respond to Resident #5’s failure to void following the removal of the resident’s catheter in a timely manner, which delayed the resident’s transfer to the hospital. Resident #5 was admitted to the facility on 9/25/25. Resident #5 was sent to the emergency department on 4/30/26 and returned the same day with an indwelling (tubing placed in the bladder) catheter for urinary retention and an order for an antibiotic. On 5/12/26 at approximately 1:30 p.m. the resident’s indwelling catheter was removed per the physician’s orders. On 5/12/26 at 7:45 p.m. Resident #5 was sitting in the dining room and told the nurse he was not feeling well. Resident #5 was escorted to his room and his vital signs were checked and within normal limits. The nurse documented the catheter had been removed earlier in the day and Resident #5 had not voided. The nurse attempted to use a bladder scan (machine to measure volume of urine in the bladder), however the bladder scan was not functioning. Resident #5’s representative arrived at the facility and voiced multiple concerns regarding Resident #5 not voiding after the catheter was removed and the green exudate (fluid) that was noted on the meatus (tip) of the resident’s penis. The nurse provided reassurance that efforts were ongoing regarding the bladder scanner and the resident’s voiding issues. The resident’s representative was informed the physician would be notified regarding the abnormal drainage and edematous (swollen) penis and lack of voiding since the resident’s indwelling catheter had been removed. However, Resident #5’s representative wanted Resident #5 sent to the emergency room and did not want to troubleshoot the issues at the facility. On 5/12/26 at 11:24 p.m. (over nine hours after the resident’s catheter was removed) Resident #5 was sent to the hospital by emergency medical transport for further evaluation per the resident’s representative’s request. At the hospital, Resident #5 was found to have a distended bladder, suprapubic cramping, a strong urge to void, and green discharge from the urethral meatus. An indwelling catheter was immediately placed with a urine output of 1300 milliliters (ml). Resident #5 was diagnosed with urethritis (inflammation of the tube that carries urine out of the body), urethral discharge and retention of urine. The resident was discharged back to the facility on 5/13/26 with a physician’s order for an antibiotic. Findings include: I. Resident #5A. Resident statusResident #5, age 78, was admitted on 9/25/25. According to the May 2026 computerized physician orders (CPO), diagnoses included cerebral infraction, Parkinson’s disease and Alzheimer’s disease. The 3/30/26 minimum data set (MDS) assessment revealed the resident was severely cognitively impaired with a brief interview for mental status (BIMS) score of three out of 15. The MDS assessment revealed the resident was dependent on staff for dressing, toilet hygiene, and personal hygiene. He was dependent on staff for transfers on and off the bed and on and off the toilet. The MDS assessment revealed the resident was incontinent of urine and did not have a catheter at the time of the assessment. B. Resident #5’s representative interviewResident #5’s representative was interviewed on 5/19/26 at 2:40 p.m. The representative said she was notified earlier in the day (on 5/12/26) , from their paid companion who sat with Resident #5 at the facility, of a discharge from Resident #5’s penis. Resident #5’s representative said she notified the director of nursing (DON) earlier in the day about the discharge and the DON told her that the discharge was normal. Resident #5’s representative said she and her husband arrived at the facility at 7:30 p.m. She said Resident #5 was in his room and said he felt lousy and was holding his lower abdomen saying it hurt. Resident #5’s representative said she asked the nurse to go to the room to look at Resident #5’s penis because of the reported green discharge. Resident #5’s representative said after they looked at the resident’s penis, she asked for the resident to be sent to the hospital because his penis looked infected to her and her husband. She said the nurse told her the facility was able to manage his care. Resident #5’s representative said she was told by the nurse that Resident #5’s bladder had been scanned twice; however, when the nurse went to scan his bladder while they were there, the nurse said the bladder scan was not functioning. Resident #5’s representative said she again requested that the resident be sent to the hospital because he had not voided or been checked in several hours and the resident was uncomfortable. She said she was told the resident did not need to go to the hospital because the facility could care for him in place. She said her husband then spoke with the DON and was told the laboratory (lab) work and a urine sample could be done at the facility. Resident #5’s representative said the resident was acting like he needed to urinate and said he was cramping up. She said her husband took a urinal and with the help of a certified nurse aide (CNA), sat Resident #5 up at the edge of the bed but after five minutes, Resident #5 could not void. Resident #5’s representative said she was provided with the option of the nursing staff performing a straight catheter (to drain the bladder) on Resident #5, but she said she did not want the facility to use a catheter at the facility due to the penis looking infected and the family wanted him at the hospital for the procedure. Resident #5’s representative said she did not call the ambulance herself because she thought the facility had to make the call and have a physician’s order for the transfer. She said a new nurse came into the resident’s room after 11:00 p.m. (on 5/12/26) and agreed Resident #5 should go to the hospital and made the transfer arrangements. Resident #5’s representative said during this time, from 7:30 p.m. until 11:00 p.m., she had asked for Resident #5 to go to the hospital but was told by the nurse and the DON that he could be treated at the facility, even after she declined to have a catheter done at the facility. C. Record reviewThe 5/12/26 nursing progress note, documented at 2:05 p.m., revealed Resident #5’s indwelling catheter had been removed per physician’s orders. Review of Resident #5’s May 2026 CPO revealed a physician’s order to discontinue the resident’s catheter and perform post-void residuals every six hours for 24 hours. If greater than 400 ml of urine remained in the bladder after voiding or no voiding in 12 hours, staff were to notify the provider for new ordersThe 5/12/26 nursing progress note, documented at 7:45 p.m., revealed Resident #5 was sitting in the dining room and told the nurse he was not feeling well. Resident #5 was escorted to his room and his vital signs were checked and were within normal limits. The nurse documented the catheter had been removed earlier in the day and Resident #5 had not voided. The nurse attempted to use a bladder scan (machine to measure volume of urine in the bladder), however the bladder scan was not functioning.-There was no documentation to indicate the physician was notified regarding the resident’s inability to void and the non-functional bladder scan machine. The 5/12/26 nursing progress note, documented at 9:00 p.m., revealed Resident #5’s representative had arrived at the facility that evening and voiced multiple concerns regarding Resident #5 not voiding after the catheter was removed and the green exudate apparent on the meatus of the resident’s penis. The nurse documented that she provided reassurance that efforts were ongoing regarding the bladder scanner, voiding issues, and all the rest and a call would be placed to the physician regarding the abnormal drainage and edematous (swollen) penis, and lack of voiding since the indwelling catheter had been removed. The 5/12/26 nursing progress note, documented at 10:40 p.m., revealed Resident #5’s representative wanted Resident #5 sent to the emergency room and did not want to troubleshoot the issues at the facility. -However, the note was documented nine hours after the indwelling catheter had been removed and Resident #5 had not voided. Resident #5 had complained of not feeling well at 7:45 p.m., almost three hours prior. The 5/12/26 nursing progress note, documented at 11:24 p.m., revealed Resident #5 was sent to the hospital by emergency medical transport per Resident #5’s representative request. A review of Resident #5’s hospital records, dated 5/12/26, revealed the resident was admitted to the hospital at 11:49 p.m. and discharged back to the facility on 5/13/26 at 7:44 a.m. with the diagnoses of urethritis, urethral discharge and retention of urine. During the hospital exam, Resident #5 was found to have a distended bladder, suprapubic cramping, a strong urge to void and green discharge from the urethral meatus. An indwelling catheter was immediately placed and immediate urine output was 1300 ml. Resident #5 was discharged back to the facility with a physician’s order for an antibiotic. II. Staff interviewsThe medical director (MD), who was Resident #5’s physician, was interviewed on 5/19/26 at 9:30 a.m. The MD said he would have expected a straight catheterization would have been performed if the resident did not void all day. He said his office was not notified until that night (5/12/26) of Resident #5 not being able to void or of the green exudate discharge from his penis. He said he was not aware the bladder scanner was not working on that day. The DON and the clinical resource nurse were interviewed together on 5/19/26 at 11:30 a.m. The DON said Resident #5 had his indwelling catheter removed (on 5/12/26) and the physician’s order said to check post-void residuals every six hours. The DON said when the nurse was going to use the bladder scan for Resident #5, the resident’s representative had come to the facility and started to ask questions. The DON said the nurse informed the representative the bladder scanner was not working and the DON was trying to obtain a bladder scanner from another facility. The DON said the family had been offered in-house interventions but the family made it clear they did not want another catheter inserted at the facility. The DON said the family did not trust the facility to manage the resident. The regional clinical nurse said Resident #5’s indwelling catheter was discontinued at 2:05 p.m. on 5/12/26, per the nurse’s progress note, however; the DON said the indwelling catheter was pulled at 1:30 p.m., not at 2:00 p.m. per the nurse’s correction. The DON and the regional clinical nurse said it could take up to an hour to get a resident ready to go to the hospital unless emergency services were called. III. Facility follow-upNursing home administrator (NHA) #1 provided additional documentation on 5/20/26 at 4:26 p.m. (after the survey exit). The additional documentation included the following:A physician’s visit progress note, dated 5/20/26 at 3:52 p.m., documented that the night Resident #5 was transferred to the hospital (5/12/26), despite needing a straight catheterization for urinary retention, this was refused by the Resident #5’s representative which led to a further delay in urinary retention until the resident was able to be treated adequately at the hospital. -However, Resident #5’s representative said she had asked for Resident #5 to be sent to the hospital earlier in the evening, more than once, because she was concerned with the possible infection in Resident #5’s penis and inserting a catheter. She said she was told by the nurse and the DON that the facility could handle Resident #5’s medical issues, although the physician’s office had not been notified until late that night (5/12/26) of Resident #5’s condition (see resident representative’s interview above).
Plan of correction · submitted by the facility
#1 Corrective Action: The facility failed to provide treatment and care in accordance with professional standards for one (#5) of six residents out of nine sample residents. Specifically, the facility failed to respond to Resident #5’s failure to void following the removal of the resident’s catheter in a timely manner, which delayed the resident’s transfer to the hospital. On 5/12/26 registered nurse (RN) assessed resident #5 and proposed to power of attorney (POA) a straight catheter be completed in order to relieve resident #5’s discomfort. However, POA declined this intervention. RN on shift attempted to assess with facility bladder scanner and noted the bladder scanner was not functioning at that time. Furthermore, medical doctor (MD) was contacted regarding resident #5 not voiding and green discharge coming from the penis. Order was received and resident #5 was sent to emergency department (ED) for further eval and treatment. Nursing home administrator (NHA) has since ordered a new bladder scanner to help prevent reoccurrence during assessments.#2 Identification of Others: The facility took the following actions to prevent any further adverse outcome. On 5/14/26 a review of all residents with catheters was conducted to ensure proper orders & care plans were in place. On 5/14/26 NHA gathered pricing for a new facility bladder scanner, in the meantime one was available from a sister facility if needed.#3 Systemic Changes: The director of nursing (DON) or designee:- On 5/14/26 an ongoing re-education on peri and catheter care was initiated to nursing staff (nurses & CNA’s[certified nurse aides]).- An ongoing re-education on 5/14/26 on facilities catheter policy was initiated.- Bladder scanner ordered to prevent re-occurrence#4 Monitoring: The DON or designee will audit a total of 2 residents 2 times a week. The audit will include date, resident name, if they have had any change in condition regarding their urinary system, if catheter care orders are in place per MD and facility protocol, if the catheter part of the resident care plan, if catheter was discontinued/were MD orders followed and a comment/education section. DON/designee will complete audits 2x week for 12 consecutive weeks. These audits will be recorded on an audit form. Discrepancies will be promptly reported to the Director of Nursing. Results of the audits will be reported monthly to the quality assurance (QA) Committee.
0760Residents are Free of Significant Med Errors▼
Findings
Based on record review and interviews, the facility failed to ensure residents were free of significant medication errors for one (#5) of six residents reviewed for medications errors out of nine sample residents. Specifically, the facility failed to ensure Resident #5 received antibiotics for a diagnosis of a urinary tract infection (UTI) per the physician’s orders. Findings include:I. Facility policy and procedure The Administration of Medications policy, dated July 2017, was provided by nursing home administrator (NHA) #1 on 5/19/26 at 4:08 p.m. The policy read in pertinent part, “Medication shall be administered as prescribed by the resident’s physician, nurse practitioner, or physician’s assistant.“Medications must be given in accordance with the resident’s service plan.“Medications must be administered in accordance with the written orders of the attending physician.“The nurse or medication technician administering the medication must record such information on the resident’s medication administration record (MAR) before administering the next resident’s medication.“Should a drug be withheld, refused, or given other than at the scheduled time, the staff administering must indicate the reason on the medication administration record (MAR). For those utilizing electronic medication administration records (eMAR), the appropriate code must be entered with any follow up documentation as appropriate for the situation.”II. Resident #5A. Resident statusResident #5, age 78, was admitted on 9/25/25. According to the May 2026 computerized physician orders (CPO), diagnoses included cerebral infraction, Parkinson’s disease, Alzheimer’s disease and neuromuscular dysfunction (affects the nerves that control voluntary muscles) of the bladder. The 3/30/26 minimum data set (MDS) assessment revealed the resident was severely cognitively impaired with a brief interview for mental status (BIMS) score of three out of 15. The MDS assessment revealed the resident was dependent on staff for dressing, toileting hygiene, personal hygiene and transfers. The MDS assessment indicated Resident #5 was incontinent of urine and did not have a catheter at the time of the assessment. B. Record reviewA review of Resident #5’s emergency room provider’s note, dated 4/30/26, revealed the resident had been in the emergency room on 4/30/26, from 8:23 a.m. until 3:08 p.m. A review of Resident #5’s electronic medical record (EMR) revealed the resident returned from the emergency room on 4/30/26 with a new physician’s order for cephalexin capsule (antibiotic) 500 milligrams (mg), give one capsule by mouth three times a day for a urinary tract infection for seven days. -A review of Resident #5’s April 2026 medication administration record (MAR) revealed the cephalexin medication was not on the MAR to be administered on 4/30/26. The 4/30/26 nursing progress note, documented at 8:55 p.m., revealed Resident #5 received the first dose of cephalexin 500 mg for the UTI.-However, the administration was not documented on the MAR (see above). The automatic medication dispensing system’s transaction by item record, provided by NHA #1 on 5/19/26 at 11:23 a.m., revealed that on 4/30/26 at 8:54 p.m. one dose of cephalexin 500 mg capsule was dispensed and the quantity that remained available in the dispensing system was four capsules. A review of Resident #5’s May 2026 MAR revealed Resident #5 received the ordered dose of cephalexin 500 mg capsule on 5/1/26 at 8:00 a.m. The automatic medication dispensing system’s transaction by item record revealed one dose of 500 mg cephalexin capsule was dispensed on 5/1/26 at 7:38 a.m. and the quantity that remained available in the dispensing system was three capsules. A review of Resident #5’s May 2026 MAR revealed Resident #5 received the ordered dose of 500 mg cephalexin capsule on 5/1/26 at 2:00 p.m. The automatic medication dispensing system’s transaction by item record revealed one dose of 500 mg cephalexin was dispensed on 5/1/26 at 1:30 p.m. and the quantity that remained available in the dispensing system was two capsules. A review of Resident #5’s May 2026 MAR revealed the 5/1/26 at 8:00 p.m. 500 mg cephalexin dose was not administered and was coded to see the progress note. The 5/1/26 medication administration progress note, documented at 7:35 p.m., revealed the 500 mg cephalexin capsule for Resident #5 was ordered. A review of Resident #5’s May 2026 MAR revealed that on 5/2/26 at 8:00 a.m. the resident received a dose of 500 mg cephalexin capsule. The automatic medication dispensing system’s transaction by item record revealed two doses of 500 mg cephalexin were dispensed on 5/2/26 at 9:06 a.m. and the remaining quantity available in the dispensing system was zero capsules. A review of Resident #5’s May 2026 MAR revealed the resident received a dose of 500 mg cephalexin capsule on 5/2/26 at 2:00 p.m. A review of Resident #5’s May 2026 MAR revealed the resident received a dose of 500 mg cephalexin capsule on 5/2/26 at 8:00 p.m.-However, according to the facility’s automatic medication dispensing system’s transaction by item record, there were no more 500 mg cephalexin capsules available for dispensing after the 5/2/26 9:06 a.m. transaction (see above). A review of Resident #5’s May 2026 MAR revealed the resident received a dose of 500 mg cephalexin capsule on 5/3/26 at 8:00 a.m.-However, the automatic medication dispensing system’s transactions by item record revealed that on 5/3/26 one dose of cephalexin 250 mg was dispensed at 8:40 a.m., which was only half the dose of the physician-ordered dose of 500 mg. A review of Resident #5’s May 2026 MAR revealed the 5/3/26 2:00 p.m. dose was left blank and did not indicate if the resident received or did not receive the antibiotic administration.-However, the automatic medication dispensing system’s transactions by item record revealed there were no more cephalexin capsules dispensed after the 250 mg cephalexin capsule at 8:40 a.m. on 5/3/26 (see above). A review of Resident #5’s May 2026 MAR revealed the resident received a dose of 500 mg cephalexin capsule on 5/3/26 at 8:00 p.m.-However, the automatic medication dispensing system’s transactions by item record revealed there were no more cephalexin capsules dispensed after the 250 mg cephalexin capsule at 8:40 a.m. on 5/3/26 (see above). A review of Resident #5’s May 2026 MAR revealed the 5/4/26 at 8:00 a.m. 500 mg cephalexin dose was not administered and coded to see the progress note. The 5/4/26 medication administration progress note, documented at 7:13 a.m., revealed the 500 mg cephalexin capsule for Resident #5 was ordered. A review of Resident #5’s May 2026 MAR revealed the 5/4/26 at 2:00 p.m. 500 mg cephalexin dose was not administered and coded to see the progress note. The 5/4/26 medication administration progress note, documented at 1:18 p.m., revealed the 500 mg cephalexin capsule for Resident #5 was ordered. A review of Resident #5’s May 2026 MAR revealed the 5/4/26 at 8:00 p.m. 500 mg cephalexin dose was not administered and coded to see the progress note. The 5/4/26 medication administration note, documented at 8:54 p.m., revealed the facility was waiting for the delivery of the 500 mg cephalexin capsules from the pharmacy and the 500 mg cephalexin capsules were not stocked in the automatic medication dispensing system. A review of Resident #5’s May 2026 MAR revealed the 5/5/26 at 8:00 a.m. 500 mg cephalexin dose was not administered and coded to see the progress note. The 5/5/26 medication administration progress note, documented at 8:09 a.m., revealed the 500 mg cephalexin capsule for Resident #5 was ordered. A review of Resident #5’s May 2026 MAR revealed the 5/5/26 at 2:00 p.m. 500 mg cephalexin dose was not administered and coded to see the progress note. The 5/5/26 medication administration progress note documented at 1:06 p.m. revealed the 500 mg cephalexin capsule for Resident #5 was ordered. A review of Resident #5’s May 2026 MAR revealed the resident received the 500 mg dose of cephalexin as ordered on 5/5/26 at 8:00 p.m., 5/6/26 at 8:00 a.m., 5/6/26 at 2:00 p.m., 5/7/26 at 8:00 p.m., 5/7/26 at 8:00 a.m., 5/7/26 at 2:00 p.m. and 5/7/26 at 8:00 p.m. A review of Resident #5’s May 2026 MAR revealed the medication was discontinued on 5/7/26 (after the 8:00 p.m. dose), at seven days, as prescribed by the physician.-However, record review revealed Resident #5 missed 10 doses (out of 21 doses) of the physician-ordered cephalexin 500 mg capsules.-Review of Resident #5’s EMR revealed no documentation to indicate that the facility had notified the physician regarding the resident’s missed doses of antibiotics on 5/1/26, 5/3/26, 5/4/26 and 5/5/26. III. Staff interviews. The facility’s medical director (MD), who was Resident #5’s physician, was interviewed on 5/19/26 at 9:30 a.m. The MD said he would expect a call if a resident’s medication was missed, especially an antibiotic. He said if he was notified, he would ask the nurse how the resident was feeling, what the resident’s vital signs were and if the resident was stable. He said he would want to know when the facility expected the medication to be delivered in order to provide further instructions to the nursing staff, such as putting a hold on the medication until it was delivered or ordering another medication. The MD said he was not aware Resident #5 had missed so many doses of the prescribed antibiotic. He said the nursing staff should follow physician’s orders and the physician should be notified of missed medications. The director of nursing (DON) and the clinical resource nurse were interviewed together on 5/19/26 at 11:30 a.m. The DON said she would expect the nursing staff to notify the physician if a resident missed a dose of medication in order to receive further instructions for that resident. The DON and the clinical resource nurse said it usually did not take several days for a medication to be delivered and could not explain why the 500 mg cephalexin was delayed for Resident #5. The DON said a blank in the MAR would indicate the medication was not administered to the resident. She said she expected her nursing staff to follow physician’s orders. The DON was interviewed again on 5/19/26 at 5:15 p.m. The DON said the infection preventionist was responsible for tracking the culture and sensitivity (C&S) (a two-part laboratory (lab) procedure used to diagnose infections and to check which medications would be effective) results and tracking the antibiotic use in the facility. The pharmacy consultant was interviewed on 5/19/26 at 5:30 p.m. The pharmacy consultant said it was important for the nursing staff to follow physician’s orders. She said if a medication was missed, the medication should be given as soon as possible and the physician should be notified of the missed medication. The pharmacy consultant said it was a joint effort between the medical provider and the facility to follow up on the C&S results in order to track if a resident was prescribed the correct antibiotic. She said the goal was for a resident to take all the doses of a prescribed medication. IV. Facility follow-upNHA #1 provided the following additional documentation on 5/20/26 at 4:26 p.m. (after the survey exit):Resident #5’s 4/30/26 urine C&S lab results were retrieved on 5/19/26 at 6:04 p.m. The report documented the lab results were completed on 5/3/26 at 8:32 a.m. The urine C&S revealed the bacteria was enterococcus faecalis (class of bacteria) and revealed cephalexin, which was ordered for Resident #5, was not susceptible (effective) to the infection. -However, the facility did not obtain Resident #5’s urine culture C&S report until after the concern for the resident’s missed doses of antibiotics was brought to the facility’s attention during the survey. The facility did not obtain the C&S report until after the survey exit and were not aware that the bacteria present in the resident’s urine was not susceptible to the initial prescribed dose of antibiotics at the time of the survey investigation. There was no indication that the MD was made of the results.
Plan of correction · submitted by the facility
#1 Corrective Action: The facility failed to ensure residents were free of significant medication errors for one (#5) of six residents reviewed for medications errors out of nine sample residents. Specifically, the facility failed to ensure Resident #5 received antibiotics for a diagnosis of a urinary tract infection (UTI) per the physician’s orders. On 5/19/26 an ongoing immediate education was initiated for nurses/med techs regarding what steps to take if a medication is unavailable. Risk incident report completed on missed doses of antibiotic with medical doctor (MD)/power of attorney (POA) notification. Resident #5 returned from the hospital on 5/13/2026. According to hospital documentation resident #5 did not have a UTI. Diagnoses were infective urethritis, penile discharge and urinary distention. Noted in the document was that enterococcus is resistant to cephalosporins like Keflex, so prior antibiotic (Keflex) likely did not treat this infection.#2 Identification of Others: The facility took the following actions to prevent any further adverse outcome. On 5/19/26 all new medications were reviewed to ensure other residents did not have missed medications. No further concerns noted.#3 Systemic Changes: The director of nursing (DON) or designee:- On 5/19/26 initiated an ongoing education with nurses on facility protocol for missing medications.- Ongoing education will continue along with audits until compliance is met.#4 Monitoring: The DON, social services director (SSD) or designee will audit 3 resident electronic medication administration record (EMAR’s) 3 times a week. The audit will include date, resident name, if any medications on the EMAR were missed, if a miss occurred was the facility protocol on missed medications followed and a section for notes/education. DON/designee will complete audits 3 x week for 12 consecutive weeks. These audits will be recorded on an audit form. Discrepancies will be promptly reported to the Director of Nursing. Results of the audits will be reported monthly to the quality assurance (QA) Committee.
0880Infection Prevention & Control▼
Findings
Based on observations and interviews, the facility failed to maintain an effective infection prevention and control program to provide a safe, sanitary, and comfortable environment to help prevent the development and transmission of disease. Specifically, the facility failed to ensure Resident #5’s indwelling catheter bag was not touching the floor. Findings include:I. Professional referenceAccording to the Centers for Disease Control and Prevention’s (CDC) Proper Techniques For Urinary Catheter Maintenance , (4/25/24), retrieved on 5/26/26, from and https://www.cdc.gov/infection-control/hcp/cauti/summary-of-recommendations.html“Keep the collecting bag below the level of the bladder at all times. Do not rest the bag on the floor.” II. Facility policy and procedureThe Infection Control Policy/Procedure, dated April 2020, was provided by nursing home administrator (NHA) #1 on 5/19/26 at 4:08 p.m. It read in pertinent part, “It is the policy of this facility to prevent the spread of bloodborne pathogens among healthcare workers by the direct or indirect contact with high risk of body fluids.“Standard precautions are the basic level of infection control that should be used in the care of all residents all of the time.“Applies to blood, all body fluids, secretions and excretions (except sweat) whether or not they contain visible blood; non-intact skin, and mucous membranes.“Resident care equipment and devices - handle in a manner that prevents transfer of microorganisms to others and to the environment.”III. ObservationsOn 5/18/26 at 11:50 a.m. Resident #5 was observed in the dining room with his catheter bag clipped to the underside of his wheelchair. The bottom of the catheter bag was sitting on the floor. There was approximately one to two inches of catheter tubing dragging on the floor. There was no privacy bag covering the catheter bag. On 5/18/26 at 12:15 p.m. Resident #5 was in his room. The resident’s catheter bag was lying flat on the floor next to the bed. There was no privacy bag covering the catheter bag. On 5/18/26 at 1:44 p.m. Resident #5 was in his room. The resident’s catheter bag had a privacy covering, however; the catheter bag was lying flat on the floor, next to the bed, with the top half of the catheter bag (where the catheter tubing entered the bag) out of the privacy bag and approximately three to four inches of the catheter tubing was lying on the floor. On 5/18/26 at 3:10 p.m. Resident # 5 was in bed with his catheter bag propped up against the bed. The bottom half of the catheter bag was out of the privacy bag and sitting on the floor mat next to the bed. IV. Staff interviewsLicensed practical nurse (LPN) #1 was interviewed on 5/18/26 at 3:22 p.m. LPN #1 said catheter bags should be checked at least every shift. She said they should be stored below the bladder and if the resident was in bed, the catheter bag should be clipped to the bed and off the floor. She said residents’ catheter bags should not be touching the floor or lying on the floor for infection control reasons. LPN #1 said catheter bags should be covered for infection control and dignity purposes. The director of nursing (DON) and the clinical resource nurse were interviewed together on 5/19/26 at 11:30 a.m. The DON said catheter bags should not be placed on the floor and should be clipped to the bed or a resident’s wheelchair to prevent infections.
Plan of correction · submitted by the facility
#1 Corrective Action: The facility failed to maintain an effective infection prevention and control program to provide a safe, sanitary, and comfortable environment to help prevent the development and transmission of disease. Specifically, the facility failed to ensure Resident #5’s indwelling catheter bag was not touching the floor. On 5/18/2026 an ongoing staff re-education was initiated regarding standard precautions and proper care of a catheter bag/tubing.#2 Identification of Others: The facility took the following actions to prevent any further adverse outcome.- On 5/19/26 infection preventionist (IP) completed an audit of all residents who had catheter bags to ensure catheter bags were present/offered, catheter positioning and tubing were in accordance with facility policy. No further concerns noted.#3 Systemic Changes: The director of nursing (DON) or designee:- On 5/18/2026 an ongoing staff re-education was initiated regarding standard precautions and proper care of a catheter bag/tubing.- IP completed a full in-house inspection to ensure catheter bags were covered and to ensure catheter bags & tubing were positioned as required per facility protocol.#4 Monitoring: The DON or designee will audit 2 residents with catheter bags 2 times weekly. The audit will include date, resident name, if catheter bag is covered, if the catheter bag positioning/tubing is acceptable per facility protocol, if infection control practices are followed and a section for notes/education. DON/designee will complete audits 2x week for 12 consecutive weeks. These audits will be recorded on an audit form. Discrepancies will be promptly reported to the Director of Nursing. Results of the audits will be reported monthly to the quality assurance (QA) Committee.
5/19/2026Licensure Complaint Survey · ID 232889-H13 deficiencies▼
0000Initial CommentsSurveyor note▼
Findings
A survey with #CO2995143 was completed on 5/18/26 to 5/19/26. Three deficiencies were cited.
Plan of correction
The state did not require a plan of correction for this citation.
0701Resident Care - Overall Care of the Residents▼
Findings
Based on record review and interviews, the facility failed to provide treatment and care in accordance with professional standards for one (#5) of six residents out of nine sample residents. Specifically, the facility failed to respond to Resident #5’s failure to void following the removal of the resident’s catheter in a timely manner, which delayed the resident’s transfer to the hospital. Resident #5 was admitted to the facility on 9/25/25. Resident #5 was sent to the emergency department on 4/30/26 and returned the same day with an indwelling (tubing placed in the bladder) catheter for urinary retention and an order for an antibiotic. On 5/12/26 at approximately 1:30 p.m. the resident’s indwelling catheter was removed per the physician’s orders. On 5/12/26 at 7:45 p.m. Resident #5 was sitting in the dining room and told the nurse he was not feeling well. Resident #5 was escorted to his room and his vital signs were checked and within normal limits. The nurse documented the catheter had been removed earlier in the day and Resident #5 had not voided. The nurse attempted to use a bladder scan (machine to measure volume of urine in the bladder), however the bladder scan was not functioning. Resident #5’s representative arrived at the facility and voiced multiple concerns regarding Resident #5 not voiding after the catheter was removed and the green exudate (fluid) that was noted on the meatus (tip) of the resident’s penis. The nurse provided reassurance that efforts were ongoing regarding the bladder scanner and the resident’s voiding issues. The resident’s representative was informed the physician would be notified regarding the abnormal drainage and edematous (swollen) penis and lack of voiding since the resident’s indwelling catheter had been removed. However, Resident #5’s representative wanted Resident #5 sent to the emergency room and did not want to troubleshoot the issues at the facility. On 5/12/26 at 11:24 p.m. (over nine hours after the resident’s catheter was removed) Resident #5 was sent to the hospital by emergency medical transport for further evaluation per the resident’s representative’s request. At the hospital, Resident #5 was found to have a distended bladder, suprapubic cramping, a strong urge to void, and green discharge from the urethral meatus. An indwelling catheter was immediately placed with a urine output of 1300 milliliters (ml). Resident #5 was diagnosed with urethritis (inflammation of the tube that carries urine out of the body), urethral discharge and retention of urine. The resident was discharged back to the facility on 5/13/26 with a physician’s order for an antibiotic. Findings include: I. Resident #5A. Resident statusResident #5, age 78, was admitted on 9/25/25. According to the May 2026 computerized physician orders (CPO), diagnoses included cerebral infraction, Parkinson’s disease and Alzheimer’s disease. The 3/30/26 comprehensive assessment revealed the resident was severely cognitively impaired. The comprehensive assessment revealed the resident was dependent on staff for dressing, toilet hygiene, and personal hygiene. He was dependent on staff for transfers on and off the bed and on and off the toilet. The comprehensive assessment revealed the resident was incontinent of urine and did not have a catheter at the time of the assessment. B. Resident #5’s representative interviewResident #5’s representative was interviewed on 5/19/26 at 2:40 p.m. The representative said she was notified earlier in the day (on 5/12/26) , from their paid companion who sat with Resident #5 at the facility, of a discharge from Resident #5’s penis. Resident #5’s representative said she notified the director of nursing (DON) earlier in the day about the discharge and the DON told her that the discharge was normal. Resident #5’s representative said she and her husband arrived at the facility at 7:30 p.m. She said Resident #5 was in his room and said he felt lousy and was holding his lower abdomen saying it hurt. Resident #5’s representative said she asked the nurse to go to the room to look at Resident #5’s penis because of the reported green discharge. Resident #5’s representative said after they looked at the resident’s penis, she asked for the resident to be sent to the hospital because his penis looked infected to her and her husband. She said the nurse told her the facility was able to manage his care. Resident #5’s representative said she was told by the nurse that Resident #5’s bladder had been scanned twice; however, when the nurse went to scan his bladder while they were there, the nurse said the bladder scan was not functioning. Resident #5’s representative said she again requested that the resident be sent to the hospital because he had not voided or been checked in several hours and the resident was uncomfortable. She said she was told the resident did not need to go to the hospital because the facility could care for him in place. She said her husband then spoke with the DON and was told the laboratory (lab) work and a urine sample could be done at the facility. Resident #5’s representative said the resident was acting like he needed to urinate and said he was cramping up. She said her husband took a urinal and with the help of a certified nurse aide (CNA), sat Resident #5 up at the edge of the bed but after five minutes, Resident #5 could not void. Resident #5’s representative said she was provided with the option of the nursing staff performing a straight catheter (to drain the bladder) on Resident #5, but she said she did not want the facility to use a catheter at the facility due to the penis looking infected and the family wanted him at the hospital for the procedure. Resident #5’s representative said she did not call the ambulance herself because she thought the facility had to make the call and have a physician’s order for the transfer. She said a new nurse came into the resident’s room after 11:00 p.m. (on 5/12/26) and agreed Resident #5 should go to the hospital and made the transfer arrangements. Resident #5’s representative said during this time, from 7:30 p.m. until 11:00 p.m., she had asked for Resident #5 to go to the hospital but was told by the nurse and the DON that he could be treated at the facility, even after she declined to have a catheter done at the facility. C. Record reviewThe 5/12/26 nursing progress note, documented at 2:05 p.m., revealed Resident #5’s indwelling catheter had been removed per physician’s orders. Review of Resident #5’s May 2026 CPO revealed a physician’s order to discontinue the resident’s catheter and perform post-void residuals every six hours for 24 hours. If greater than 400 ml of urine remained in the bladder after voiding or no voiding in 12 hours, staff were to notify the provider for new ordersThe 5/12/26 nursing progress note, documented at 7:45 p.m., revealed Resident #5 was sitting in the dining room and told the nurse he was not feeling well. Resident #5 was escorted to his room and his vital signs were checked and were within normal limits. The nurse documented the catheter had been removed earlier in the day and Resident #5 had not voided. The nurse attempted to use a bladder scan (machine to measure volume of urine in the bladder), however the bladder scan was not functioning.-There was no documentation to indicate the physician was notified regarding the resident’s inability to void and the non-functional bladder scan machine. The 5/12/26 nursing progress note, documented at 9:00 p.m., revealed Resident #5’s representative had arrived at the facility that evening and voiced multiple concerns regarding Resident #5 not voiding after the catheter was removed and the green exudate apparent on the meatus of the resident’s penis. The nurse documented that she provided reassurance that efforts were ongoing regarding the bladder scanner, voiding issues, and all the rest and a call would be placed to the physician regarding the abnormal drainage and edematous (swollen) penis, andlack of voiding since the indwelling catheter had been removed. The 5/12/26 nursing progress note, documented at 10:40 p.m., revealed Resident #5’s representative wanted Resident #5 sent to the emergency room and did not want to troubleshoot the issues at the facility. -However, the note was documented nine hours after the indwelling catheter had been removed and Resident #5 had not voided. Resident #5 had complained of not feeling well at 7:45 p.m., almost three hours prior. The 5/12/26 nursing progress note, documented at 11:24 p.m., revealed Resident #5 was sent to the hospital by emergency medical transport per Resident #5’s representative request. A review of Resident #5’s hospital records, dated 5/12/26, revealed the resident was admitted to the hospital at 11:49 p.m. and discharged back to the facility on 5/13/26 at 7:44 a.m. with the diagnoses of urethritis, urethral discharge and retention of urine. During the hospital exam, Resident #5 was found to have a distended bladder, suprapubic cramping, a strong urge to void and green discharge from the urethral meatus. An indwelling catheter was immediately placed and immediate urine output was 1300 ml. Resident #5 was discharged back to the facility with a physician’s order for an antibiotic. II. Staff interviewsThe medical director (MD), who was Resident #5’s physician, was interviewed on 5/19/26 at 9:30 a.m. The MD said he would have expected a straight catheterization would have been performed if the resident did not void all day. He said his office was not notified until that night (5/12/26) of Resident #5 not being able to void or of the green exudate discharge from his penis. He said he was not aware the bladder scanner was not working on that day. The DON and the clinical resource nurse were interviewed together on 5/19/26 at 11:30 a.m. The DON said Resident #5 had his indwelling catheter removed (on 5/12/26) and the physician’s order said to check post-void residuals every six hours. The DON said when the nurse was going to use the bladder scan for Resident #5, the resident’s representative had come to the facility and started to ask questions. The DON said the nurse informed the representative the bladder scanner was not working and the DON was trying to obtain a bladder scanner from another facility. The DON said the family had been offered in-house interventions but the family made it clear they did not want another catheter inserted at the facility. The DON said the family did not trust the facility to manage the resident. The regional clinical nurse said Resident #5’s indwelling catheter was discontinued at 2:05 p.m. on 5/12/26, per the nurse’s progress note, however; the DON said the indwelling catheter was pulled at 1:30 p.m., not at 2:00 p.m. per the nurse’s correction. The DON and the regional clinical nurse said it could take up to an hour to get a resident ready to go to the hospital unless emergency services were called. III. Facility follow-upNursing home administrator (NHA) #1 provided additional documentation on 5/20/26 at 4:26 p.m. (after the survey exit). The additional documentation included the following:A physician’s visit progress note, dated 5/20/26 at 3:52 p.m., documented that the night Resident #5 was transferred to the hospital (5/12/26), despite needing a straight catheterization for urinary retention, this was refused by the Resident #5’s representative which led to a further delay in urinary retention until the resident was able to be treated adequately at the hospital. -However, Resident #5’s representative said she had asked for Resident #5 to be sent to the hospital earlier in the evening, more than once, because she was concerned with the possible infection in Resident #5’s penis and inserting a catheter. She said she was told by the nurse and the DON that the facility could handle Resident #5’s medical issues, although the physician’s office had not been notified until late that night (5/12/26) of Resident #5’s condition (see resident representative’s interview above).
Plan of correction · submitted by the facility
#1 Corrective Action: The facility failed to provide treatment and care in accordance with professional standards for one (#5) of six residents out of nine sample residents. Specifically, the facility failed to respond to Resident #5’s failure to void following the removal of the resident’s catheter in a timely manner, which delayed the resident’s transfer to the hospital. On 5/12/26 registered nurse (RN) assessed resident #5 and proposed to POA a straight catheter be completed in order to relieve resident #5’s discomfort. However, power of attorney (POA) declined this intervention. RN on shift attempted to assess with facility bladder scanner and noted the bladder scanner was not functioning at that time. Furthermore, medical doctor (MD) was contacted regarding resident #5 not voiding and green discharge coming from the penis. Order was received and resident #5 was sent to emergency department (ED) for further eval and treatment. Nursing home administrator (NHA) has since ordered a new bladder scanner to help prevent reoccurrence during assessments.#2 Identification of Others: The facility took the following actions to prevent any further adverse outcome. On 5/14/26 a review of all residents with catheters was conducted to ensure proper orders & care plans were in place. On 5/14/26 NHA gathered pricing for a new facility bladder scanner, in the meantime one was available from a sister facility if needed.#3 Systemic Changes: The director of nursing (DON) or designee:- On 5/14/26 an ongoing re-education on peri and catheter care was initiated to nursing staff (nurses & CNA’s [certified nurse aides]).- An ongoing re-education on 5/14/26 on facilities catheter policy was initiated.- Bladder scanner ordered to prevent re-occurrence#4 Monitoring: The DON or designee will audit a total of 2 residents 2 times a week. The audit will include date, resident name, if they have had any change in condition regarding their urinary system, if catheter care orders are in place per MD and facility protocol, if the catheter part of the resident care plan, if catheter was discontinued/were MD orders followed and a comment/education section. DON/designee will complete audits 2x week for 12 consecutive weeks. These audits will be recorded on an audit form. Discrepancies will be promptly reported to the Director of Nursing. Results of the audits will be reported monthly to the quality assurance (QA) Committee.
0923Nursing Services - Medication Administration▼
Findings
Based on record review and interviews, the facility failed to ensure residents were free of significant medication errors for one (#5) of six residents reviewed for medications errors out of nine sample residents. Specifically, the facility failed to ensure Resident #5 received antibiotics for a diagnosis of a urinary tract infection (UTI) per the physician’s orders. Findings include:I. Facility policy and procedure The Administration of Medications policy, dated July 2017, was provided by nursing home administrator (NHA) #1 on 5/19/26 at 4:08 p.m. The policy read in pertinent part, “Medication shall be administered as prescribed by the resident’s physician, nurse practitioner, or physician’s assistant.“Medications must be given in accordance with the resident’s service plan.“Medications must be administered in accordance with the written orders of the attending physician.“The nurse or medication technician administering the medication must record such information on the resident’s medication administration record (MAR) before administering the next resident’s medication.“Should a drug be withheld, refused, or given other than at the scheduled time, the staff administering must indicate the reason on the medication administration record (MAR). For those utilizing electronic medication administration records (eMAR), the appropriate code must be entered with any follow up documentation as appropriate for the situation.”II. Resident #5A. Resident statusResident #5, age 78, was admitted on 9/25/25. According to the May 2026 computerized physician orders (CPO), diagnoses included cerebral infraction, Parkinson’s disease, Alzheimer’s disease and neuromuscular dysfunction (affects the nerves that control voluntary muscles) of the bladder. The 3/30/26 comprehensive assessment revealed the resident was severely cognitively impaired. The comprehensive assessment revealed the resident was dependent on staff for dressing, toileting hygiene, personal hygiene and transfers. The comprehensive assessment indicated Resident #5 was incontinent of urine and did not have a catheter at the time of the assessment. B. Record reviewA review of Resident #5’s emergency room provider’s note, dated 4/30/26, revealed the resident had been in the emergency room on 4/30/26, from 8:23 a.m. until 3:08 p.m. A review of Resident #5’s electronic medical record (EMR) revealed the resident returned from the emergency room on 4/30/26 with a new physician’s order for cephalexin capsule (antibiotic) 500 milligrams (mg), give one capsule by mouth three times a day for a urinary tract infection for seven days. -A review of Resident #5’s April 2026 medication administration record (MAR) revealed the cephalexin medication was not on the MAR to be administered on 4/30/26. The 4/30/26 nursing progress note, documented at 8:55 p.m., revealed Resident #5 received the first dose of cephalexin 500 mg for the UTI.-However, the administration was not documented on the MAR (see above). The automatic medication dispensing system’s transaction by item record, provided by NHA #1 on 5/19/26 at 11:23 a.m., revealed that on 4/30/26 at 8:54 p.m. one dose of cephalexin 500 mg capsule was dispensed and the quantity that remained available in the dispensing system was four capsules. A review of Resident #5’s May 2026 MAR revealed Resident #5 received the ordered dose of cephalexin 500 mg capsule on 5/1/26 at 8:00 a.m. The automatic medication dispensing system’s transaction by item record revealed one dose of 500 mg cephalexin capsule was dispensed on 5/1/26 at 7:38 a.m. and the quantity that remained available in the dispensing system was three capsules. A review of Resident #5’s May 2026 MAR revealed Resident #5 received the ordered dose of 500 mg cephalexin capsule on 5/1/26 at 2:00 p.m. The automatic medication dispensing system’s transaction by item record revealed one dose of 500 mg cephalexin was dispensed on 5/1/26 at 1:30 p.m. and the quantity that remained available in the dispensing system was two capsules. A review of Resident #5’s May 2026 MAR revealed the 5/1/26 at 8:00 p.m. 500 mg cephalexin dose was not administered and was coded to see the progress note. The 5/1/26 medication administration progress note, documented at 7:35 p.m., revealed the 500 mg cephalexin capsule for Resident #5 was ordered. A review of Resident #5’s May 2026 MAR revealed that on 5/2/26 at 8:00 a.m. the resident received a dose of 500 mg cephalexin capsule. The automatic medication dispensing system’s transaction by item record revealed two doses of 500 mg cephalexin were dispensed on 5/2/26 at 9:06 a.m. and the remaining quantity available in the dispensing system was zero capsules. A review of Resident #5’s May 2026 MAR revealed the resident received a dose of 500 mg cephalexin capsule on 5/2/26 at 2:00 p.m. A review of Resident #5’s May 2026 MAR revealed the resident received a dose of 500 mg cephalexin capsule on 5/2/26 at 8:00 p.m.-However, according to the facility’s automatic medication dispensing system’s transaction by item record, there were no more 500 mg cephalexin capsules available for dispensing after the 5/2/26 9:06 a.m. transaction (see above). A review of Resident #5’s May 2026 MAR revealed the resident received a dose of 500 mg cephalexin capsule on 5/3/26 at 8:00 a.m.-However, the automatic medication dispensing system’s transactions by item record revealed that on 5/3/26 one dose of cephalexin 250 mg was dispensed at 8:40 a.m., which was only half the dose of the physician-ordered dose of 500 mg. A review of Resident #5’s May 2026 MAR revealed the 5/3/26 2:00 p.m. dose was left blank and did not indicate if the resident received or did not receive the antibiotic administration.-However, the automatic medication dispensing system’s transactions by item record revealed there were no more cephalexin capsules dispensed after the 250 mg cephalexin capsule at 8:40 a.m. on 5/3/26 (see above). A review of Resident #5’s May 2026 MAR revealed the resident received a dose of 500 mg cephalexin capsule on 5/3/26 at 8:00 p.m.-However, the automatic medication dispensing system’s transactions by item record revealed there were no more cephalexin capsules dispensed after the 250 mg cephalexin capsule at 8:40 a.m. on 5/3/26 (see above). A review of Resident #5’s May 2026 MAR revealed the 5/4/26 at 8:00 a.m. 500 mg cephalexin dose was not administered and coded to see the progress note. The 5/4/26 medication administration progress note, documented at 7:13 a.m., revealed the 500 mg cephalexin capsule for Resident #5 was ordered. A review of Resident #5’s May 2026 MAR revealed the 5/4/26 at 2:00 p.m. 500 mg cephalexin dose was not administered and coded to see the progress note. The 5/4/26 medication administration progress note, documented at 1:18 p.m., revealed the 500 mg cephalexin capsule for Resident #5 was ordered. A review of Resident #5’s May 2026 MAR revealed the 5/4/26 at 8:00 p.m. 500 mg cephalexin dose was not administered and coded to see the progress note. The 5/4/26 medication administration note, documented at 8:54 p.m., revealed the facility was waiting for the delivery of the 500 mg cephalexin capsules from the pharmacy and the 500 mg cephalexin capsules were not stocked in the automatic medication dispensing system. A review of Resident #5’s May 2026 MAR revealed the 5/5/26 at 8:00 a.m. 500 mg cephalexin dose was not administered and coded to see the progress note. The 5/5/26 medication administration progress note, documented at 8:09 a.m., revealed the 500 mg cephalexin capsule for Resident #5 was ordered. A review of Resident #5’s May 2026 MAR revealed the 5/5/26 at 2:00 p.m. 500 mg cephalexin dose was not administered and coded to see the progress note. The 5/5/26 medication administration progress note documented at 1:06 p.m. revealed the 500 mg cephalexin capsule for Resident #5 was ordered. A review of Resident #5’s May 2026 MAR revealed the resident received the 500 mg dose of cephalexin as ordered on 5/5/26 at 8:00 p.m., 5/6/26 at 8:00 a.m., 5/6/26 at 2:00 p.m., 5/7/26 at 8:00 p.m., 5/7/26 at 8:00 a.m., 5/7/26 at 2:00 p.m. and 5/7/26 at 8:00 p.m. A review of Resident #5’s May 2026 MAR revealed the medication was discontinued on 5/7/26 (after the 8:00 p.m. dose), at seven days, as prescribed by the physician.-However, record review revealed Resident #5 missed 10 doses (out of 21 doses) of the physician-ordered cephalexin 500 mg capsules.-Review of Resident #5’s EMR revealed no documentation to indicate that the facility had notified the physician regarding the resident’s missed doses of antibiotics on 5/1/26, 5/3/26, 5/4/26 and 5/5/26. III. Staff interviews. The facility’s medical director (MD), who was Resident #5’s physician, was interviewed on 5/19/26 at 9:30 a.m. The MD said he would expect a call if a resident’s medication was missed, especially an antibiotic. He said if he was notified, he would ask the nurse how the resident was feeling, what the resident’s vital signs were and if the resident was stable. He said he would want to know when the facility expected the medication to be delivered in order to provide further instructions to the nursing staff, such as putting a hold on the medication until it was delivered or ordering another medication. The MD said he was not aware Resident #5 had missed so many doses of the prescribed antibiotic. He said the nursing staff should follow physician’s orders and the physician should be notified of missed medications. The director of nursing (DON) and the clinical resource nurse were interviewed together on 5/19/26 at 11:30 a.m. The DON said she would expect the nursing staff to notify the physician if a resident missed a dose of medication in order to receive further instructions for that resident. The DON and the clinical resource nurse said it usually did not take several days for a medication to be delivered and could not explain why the 500 mg cephalexin was delayed for Resident #5. The DON said a blank in the MAR would indicate the medication was not administered to the resident. She said she expected her nursing staff to follow physician’s orders. The DON was interviewed again on 5/19/26 at 5:15 p.m. The DON said the infection preventionist was responsible for tracking the culture and sensitivity (C&S) (a two-part laboratory (lab) procedure used to diagnose infections and to check which medications would be effective) results and tracking the antibiotic use in the facility. The pharmacy consultant was interviewed on 5/19/26 at 5:30 p.m. The pharmacy consultant said it was important for the nursing staff to follow physician’s orders. She said if a medication was missed, the medication should be given as soon as possible and the physician should be notified of the missed medication. The pharmacy consultant said it was a joint effort between the medical provider and the facility to follow up on the C&S results in order to track if a resident was prescribed the correct antibiotic. She said the goal was for a resident to take all the doses of a prescribed medication. IV. Facility follow-upNHA #1 provided the following additional documentation on 5/20/26 at 4:26 p.m. (after the survey exit):Resident #5’s 4/30/26 urine C&S lab results were retrieved on 5/19/26 at 6:04 p.m. The report documented the lab results were completed on 5/3/26 at 8:32 a.m. The urine C&S revealed the bacteria was enterococcus faecalis (class of bacteria) and revealed cephalexin, which was ordered for Resident #5, was not susceptible (effective) to the infection. -However, the facility did not obtain Resident #5’s urine culture C&S report until after the concern for the resident’s missed doses of antibiotics was brought to the facility’s attention during the survey. The facility did not obtain the C&S report until after the survey exit and were not aware that the bacteria present in the resident’s urine was not susceptible to the initial prescribed dose of antibiotics at the time of the survey investigation. There was no indication that the MD was made of the results.
Plan of correction · submitted by the facility
#1 Corrective Action: The facility failed to ensure residents were free of significant medication errors for one (#5) of six residents reviewed for medications errors out of nine sample residents. Specifically, the facility failed to ensure Resident #5 received antibiotics for a diagnosis of a urinary tract infection (UTI) per the physician’s orders. On 5/19/26 an ongoing immediate education was initiated for nurses/med techs regarding what steps to take if a medication is unavailable. Risk incident report completed on missed doses of antibiotic with medical doctor (MD)/power of attorney (POA) notification. Resident #5 returned from the hospital on 5/13/2026. According to hospital documentation resident #5 did not have a UTI. Diagnoses were infective urethritis, penile discharge and urinary distention. Noted in the document was that enterococcus is resistant to cephalosporins like Keflex, so prior antibiotic (Keflex) likely did not treat this infection.#2 Identification of Others: The facility took the following actions to prevent any further adverse outcome. On 5/19/26 all new medications were reviewed to ensure other residents did not have missed medications. No further concerns noted.#3 Systemic Changes: The director of nursing (DON) or designee:- On 5/19/26 initiated an ongoing education with nurses on facility protocol for missing medications.- Ongoing education will continue along with audits until compliance is met.#4 Monitoring: The DON, social services director (SSD) or designee will audit 3 resident electronic medication administration records (EMAR’s) 3 times a week. The audit will include date, resident name, if any medications on the EMAR were missed, if a miss occurred was the facility protocol on missed medications followed and a section for notes/education. DON/designee will complete audits 3 x week for 12 consecutive weeks. These audits will be recorded on an audit form. Discrepancies will be promptly reported to the Director of Nursing. Results of the audits will be reported monthly to the quality assurance (QA) Committee.
2603Infection Control▼
Findings
Based on observations and interviews, the facility failed to maintain an effective infection prevention and control program to provide a safe, sanitary, and comfortable environment to help prevent the development and transmission of disease. Specifically, the facility failed to ensure Resident #5’s indwelling catheter bag was not touching the floor. Findings include:I. Professional referenceAccording to the Centers for Disease Control and Prevention’s (CDC) Proper Techniques For Urinary Catheter Maintenance , (4/25/24), retrieved on 5/26/26, from and https://www.cdc.gov/infection-control/hcp/cauti/summary-of-recommendations.html“Keep the collecting bag below the level of the bladder at all times. Do not rest the bag on the floor.” II. Facility policy and procedureThe Infection Control Policy/Procedure, dated April 2020, was provided by nursing home administrator (NHA) #1 on 5/19/26 at 4:08 p.m. It read in pertinent part, “It is the policy of this facility to prevent the spread of bloodborne pathogens among healthcare workers by the direct or indirect contact with high risk of body fluids.“Standard precautions are the basic level of infection control that should be used in the care of all residents all of the time.“Applies to blood, all body fluids, secretions and excretions (except sweat) whether or not they contain visible blood; non-intact skin, and mucous membranes.“Resident care equipment and devices - handle in a manner that prevents transfer of microorganisms to others and to the environment.”III. ObservationsOn 5/18/26 at 11:50 a.m. Resident #5 was observed in the dining room with his catheter bag clipped to the underside of his wheelchair. The bottom of the catheter bag was sitting on the floor. There was approximately one to two inches of catheter tubing dragging on the floor. There was no privacy bag covering the catheter bag. On 5/18/26 at 12:15 p.m. Resident #5 was in his room. The resident’s catheter bag was lying flat on the floor next to the bed. There was no privacy bag covering the catheter bag. On 5/18/26 at 1:44 p.m. Resident #5 was in his room. The resident’s catheter bag had a privacy covering, however; the catheter bag was lying flat on the floor, next to the bed, with the top half of the catheter bag (where the catheter tubing entered the bag) out of the privacy bag and approximately three to four inches of the catheter tubing was lying on the floor. On 5/18/26 at 3:10 p.m. Resident # 5 was in bed with his catheter bag propped up against the bed. The bottom half of the catheter bag was out of the privacy bag and sitting on the floor mat next to the bed. IV. Staff interviewsLicensed practical nurse (LPN) #1 was interviewed on 5/18/26 at 3:22 p.m. LPN #1 said catheter bags should be checked at least every shift. She said they should be stored below the bladder and if the resident was in bed, the catheter bag should be clipped to the bed and off the floor. She said residents’ catheter bags should not be touching the floor or lying on the floor for infection control reasons. LPN #1 said catheter bags should be covered for infection control and dignity purposes. The director of nursing (DON) and the clinical resource nurse were interviewed together on 5/19/26 at 11:30 a.m. The DON said catheter bags should not be placed on the floor and should be clipped to the bed or a resident’s wheelchair to prevent infections.
Plan of correction · submitted by the facility
#1 Corrective Action: The facility failed to maintain an effective infection prevention and control program to provide a safe, sanitary, and comfortable environment to help prevent the development and transmission of disease. Specifically, the facility failed to ensure Resident #5’s indwelling catheter bag was not touching the floor. On 5/18/2026 an ongoing staff re-education was initiated regarding standard precautions and proper care of a catheter bag/tubing.#2 Identification of Others: The facility took the following actions to prevent any further adverse outcome.- On 5/19/26 infection preventionist (IP) completed an audit of all residents who had catheter bags to ensure catheter bags were present/offered, catheter positioning and tubing were in accordance with facility policy. No further concerns noted.#3 Systemic Changes: The director of nursing (DON) or designee:- On 5/18/2026 an ongoing staff re-education was initiated regarding standard precautions and proper care of a catheter bag/tubing.- IP completed a full in-house inspection to ensure catheter bags were covered and to ensure catheter bags & tubing were positioned as required per facility protocol.#4 Monitoring: The DON or designee will audit 2 residents with catheter bags 2 times weekly. The audit will include date, resident name, if catheter bag is covered, if the catheter bag positioning/tubing is acceptable per facility protocol, if infection control practices are followed and a section for notes/education. DON/designee will complete audits 2 x week for 12 consecutive weeks. These audits will be recorded on an audit form. Discrepancies will be promptly reported to the Director of Nursing. Results of the audits will be reported monthly to the quality assurance (QA) Committee.
2/10/2026Recertification Survey · ID 1E05DD-L112 deficiencies▼
0000INITIAL COMMENTSSurveyor note▼
Findings
INITIAL COMMENTS (ID Prefix Tag #K000) are informational only and a representation of the facility's general characteristics. This survey was conducted in accordance with the Federal Register at Section 42 CFR 483.70(a). The facility is a one (1) story, Type V (000) (V B) slab on grade construction without a basement. The facility is licensed for 104 beds and the census on the date of the survey was 84. The facility was constructed in 1970. The facility is fully protected throughout by a National Fire Protection Association (NFPA) 13 automatic fire sprinkler system that consists of a wet fire sprinkler system and 1 antifreeze system. This survey was conducted on February 10, 2026, for compliance with the National Fire Protection Association, (NFPA 101) Life Safety Code (2012) Chapter 19 "Existing Health Care Occupancies."
Plan of correction
The state did not require a plan of correction for this citation.
0161Building Construction Type and Height▼
Findings
Through record review and interview, the facility did not maintain construction, smoke and fire barriers in accordance with NFPA 101, Life Safety Code (12). Findings Include:During the record review, observations and interviews with the maintenance director could not provide the facility's life safety plans during the survey. Without an accurate copy of the life safety plans. We can not verify that the construction type, fire, and smoke barriers are being maintained within the facility. Regulatory Guidance: We would need to add the ones that applyCalifornia patch and not fully fire stopped in above ceiling not known without plans whether fire rated assembly Regulatory Reference: NFPA 101 20124.5.8 Maintenance. Whenever or wherever any device, equipment, system, condition, arrangement, level of protection, or any other feature is required for compliance with the provisions of this Code, such device, equipment, system, condition, arrangement, level of protection, or other feature shall thereafter be maintained, unless the Code exempts such maintenance. 4.2.1 Occupant Protection. A structure shall be designed, constructed, and maintained to protect occupants who are not intimate with the initialfire development for the time needed to evacuate, relocate, or defend in place 4.2.3 Systems Effectiveness. Systems utilized to achieve the goals of Section 4.1 shall be effective in mitigating the hazard or condition for which they are being used, shall be reliable, shall be maintained to the level at which they were designed to operate, andshall remain operational. 4.5.5* Situation Awareness. Systems used to achieve the goals of Section 4.1 shall be effective in facilitating and enhancing situation awareness, as appropriate, by building management, other occupants and emergency responders of the functionality or state of critical building systems, the conditions that might warrant emergency response, and the appropriate nature and timing of such responses. 4.5.7 System Design/Installation. Any fire protection system, building service equipment, feature of protection, or safeguard provided to achieve thegoals of this Code shall be designed, installed, and approved in accordance with applicable NFPA standards. 4.6.1.2Any requirements that are essential for the safety of building occupants and that are not specifically provided for by this Code shall be determined by the authority having jurisdiction. 4.6.8 Provisions in Excess of Code Requirements. Nothing in this Code shall be construed to prohibit a better building construction type, an additional means of egress, or an otherwise safer condition than that specified by the minimum requirements of this Code. 4.6.12 Maintenance, Inspection, and Testing. 4.6.12.1 Whenever or wherever any device, equipment, system, condition, arrangement, level of protection, fire-resistive construction, or any other feature is required for compliance with the provisions of this Code, such device, equipment, system, condition, arrangement, level of protection, fire-resistive construction, or other feature shall thereafter be continuously maintained. Maintenance shall be provided in accordance with applicable NFPA requirements or requirements developed as part of a performance-based design, or as directed by the authority having jurisdiction. 4.6.12.4 Any device, equipment, system, condition, arrangement, level of protection, fire-resistive construction, or any other feature requiring periodic testing, inspection, or operation to ensure its maintenance shall be tested, inspected, or operated as specified elsewhere in this Code or as directed by the authority having jurisdiction. This deficiency has the potential to affect all smoke compartments within the facility, and all residents, visitors, and staff. The deficiency was discussed with the life and safety maintenance resource advisor and the maintenance director during the survey exit conference.
Plan of correction · submitted by the facility
K161Building Construction Type and HeightResident Specific: No residents Identified but could affect all residents, staff and visitors within the facility. Identification of others: Potential to affect all occupants, who might include staff, residents and visitors. System and Measures: Through record review and interview, the facility did not maintain construction, smoke and fire barriers in accordance with NFPA 101, Life Safety Code (12). Findings Include:1. During the record review, observations and interviews with the maintenance director could not provide the facility's life safety plans during the survey. Without an accurate copy of the life safety plans. We cannot verify that the construction type, fire, and smoke barriers are being maintained within the facility. Regulatory Guidance: We would need to add the ones that apply. 2. California patch and not fully fire stopped in above ceiling not known without plans whether fire rated assembly. The facility will be asking for a time limit waiver so we can get the Life Safety plans per the guidance from Life Safety. The California patch is going to be repaired by the maintenance team to be a proper patch. Monitoring: Maintenance will check the rest of the facility for California patches and also maintain the Life Safety plans once they are received. In compliance on: 4/20/2026
0211Means of Egress - General▼
Findings
Based on observation and staff interviews, it was determined that the facility failed to arrange and maintain the means of egress in accordance with Life Safety Code Section 19.2 and Chapter 7. Findings Include:Exit gate not properly marked leading to exit passageway from courtyard of memory care Regulatory Reference: NFPA 101 20127.10.1.1 Where Required. Means of egress shall be marked in accordance with Section 7.10 where required in Chapters 11 through 43. 7.10.1.2 Exits. 7.10.1.2.1* Exits, other than main exterior exit doors that obviously and clearly are identifiable as exits, shall be marked by an approved sign that is readily visible from any direction of exit access. This deficiency has the potential to affect approximately 40 residents within the facility, and visitors, and staff. The deficiency was discussed with the life and safety maintenance resource advisor and the maintenance director during the survey exit conference.
Plan of correction · submitted by the facility
K211Means of Egress – GeneralResident Specific: No residents Identified but could affect all residents, staff and visitors within the facility. Identification of others: Potential to affect all occupants, who might include staff, residents and visitors. System and Measures: Based on observation and staff interviews, it was determined that the facility failed to arrange and maintain the means of egress in accordance with Life Safety Code Section 19.2 and Chapter 7. Findings Include:1. Exit gate not properly marked leading to exit passageway from courtyard of memory careMaintenance has ordered illuminating exit signs for the gates and will install them once received. Monitoring: Maintenance will check the exit signs along with the rest of the exit signs monthly. In compliance on: 3/9/26
0223Doors with Self-Closing Devices▼
Findings
Based on observation and staff interviews, it was determined that the facility failed to arrange and maintain the means of egress in accordance with Life Safety Section 19.3.2.1 Findings Include:Kitchen door being propped open by rise in floor which does not release without manual manipulation Regulatory Reference: NFPA 101 201219.2.2.2.7*Any door in an exit passageway, stairway enclosure, horizontal exit, smoke barrier, or hazardous area enclosure shall be permitted to be held open only by an automatic release device that complies with 7.2.1.8.2. The automatic sprinkler system, if provided, and the fire alarm system, and the systems required by 7.2.1.8.2, shall be arranged to initiate the closing action of all such doors throughout the smoke compartment or throughout the entire facility. 7.2.1.8.2 In any building of low or ordinary hazard contents, as defined in 6.2.2.2 and 6.2.2.3, or where approved by the authority having jurisdiction, door leaves shall be permitted to be automatic-closing, provided that all of the following criteria are met:Upon release of the hold-open mechanism, the leaf becomes self-closing. The release device is designed so that the leaf instantly releases manually and, upon release, becomes self-closing, or the leaf can be readily closed. The automatic releasing mechanism or medium is activated by the operation of approved smoke detectors installed in accordance with the requirements for smoke detectors for door leaf release service in NFPA 72, National Fire Alarm and Signaling Code. Upon loss of power to the hold-open device, the hold-open mechanism is released and the door leaf becomes self-closing. The release by means of smoke detection of one door leaf in a stair enclosure results in closing all door leaves serving that stair. This deficiency has the potential to affect approximately 20 residents within the facility, and visitors, and staff. The deficiency was discussed with the life and safety maintenance resource advisor and the maintenance director during the survey exit conference.
Plan of correction · submitted by the facility
K223Doors with Self-Closing DevicesResident Specific: No residents Identified but could affect all residents, staff and visitors within the facility. Identification of others: Potential to affect all occupants, who might include staff, residents and visitors. System and Measures: Based on observation and staff interviews, it was determined that the facility failed to arrange and maintain the means of egress in accordance with Life Safety Section 19.3.2.1Findings Include:1. Kitchen door being propped open by rise in floor which does not release without manual manipulationMaintenance will repair door so that it does not drag onto the floor, allowing the door to stay open. Monitoring: Maintenance will confirm that the door is opening and closing properly and do monthly door audits along with the rest of the building. In compliance on: 3/9/26
0351Sprinkler System - Installation▼
Findings
Based on record review, observation and staff interview, it was determined that the facility failed to maintain the automatic sprinkler system in accordance with National Fire Protection Association (NFPA) Standard 25 and NFPA 101 2012. Findings include: Sunrise A North Canopy “No information placard is posted listing the solution of the system and how many gallons of antifreeze system is holding” - Mountain View North Women’s hydraulic name plate. “Appears to be missing”Visual no hydro calc plate seenLast test for antifreeze testing was 2024 Regulatory Reference: NFPA 101 20125.2.6* Hydraulic Design Information Sign. The hydraulic design information sign for hydraulically designed systems shall be inspected quarterly to verify that it is attached securely to the sprinkler riser and is legible NFPA 13, 2013 Edition, Chapter 25, Section 25.5.1. The installing contractor shall identify a hydraulically designed sprinkler system with a permanently marked weatherproof metal or rigid plastic sign secured with corrosion resistant wire, chain, or other approved means. Such signs shall be placed at the alarm valve, dry pipe valve, preaction valve, or deluge valve supplying the corresponding hydraulically designed area. NFPA 254.1.8 Information Sign. 4.1.8.1 A permanently marked metal or rigid plastic information sign shall be placed at the system control riser supplying an antifreeze loop, dry system, preaction system, or auxiliary system control valve. 4.1.8.2 Each sign shall be secured with a corrosion-resistant wire, chain, or other approved means and shall indicate at least the following information:(1)Location of the area served by the system(2)Location of auxiliary drains and low-point drains for dry pipe and preaction systems(3)The presence and location of antifreeze or other auxiliary systems(4)The presence and location(s) of heat tape19.3.5.3 Where required by 19.1.6, buildings containing hospitals or limited care facilities shall be protected throughout by an approved, supervised automatic sprinkler system in accordance with Section 9.7, unless otherwise permitted by 19.3.5.5.5.3.4* Antifreeze Systems. Annually, before the onset of freezing weather, the antifreeze solution shall be tested using the following procedure:Using installation records, maintenance records, information from the owner, chemical tests, or other reliable sources of information, the type of antifreeze in the system shall be determined. If the type of antifreeze is found to be a type that is no longer permitted, the system shall be drained completely and replaced with an acceptable solution. If the type of antifreeze cannot be reliably determined, then the system shall be drained completely and replaced with an acceptable solution.(2) If the antifreeze is not replaced in accordance with step 1, test samples shall be taken at the top of each system and at the bottom of each system. If the most remote portion of the system is not near the top or the bottom of the system, an additional sample shall be taken at the most remote portion. If the connection to the water supply piping is not near the top or the bottom of the system, an additional sample shall be taken at the connection to the water supply.(3) The specific gravity of each solution shall be checked using a hydrometer with a suitable scale or a refractometer having a scale calibrated for the antifreeze solution.(4) If any of the samples exhibits a concentration in excess of what is permitted by NFPA 25, the system shall be emptied and refilled with a new acceptable solution. If a concentration greater than what is currently permitted by NFPA 25 was necessary to keep the fluid from freezing, alternate methods of preventing the pipe from freezing shall be employed.(5) If any of the samples exhibits a concentration lower than what is necessary to keep the fluid from freezing, the system shall be emptied and refilled with a new acceptable solution. This deficiency has the potential to affect all smoke compartments within the facility, and all residents, visitors, and staff. The deficiency was discussed with the life and safety maintenance resource advisor and the maintenance director during the survey exit conference.
Plan of correction · submitted by the facility
K351Sprinkler System – InstallationResident Specific: No residents Identified but could affect all residents, staff and visitors within the facility. Identification of others: Potential to affect all occupants, who might include staff, residents and visitors. System and Measures: Based on record review, observation and staff interview, it was determined that the facility failed to maintain the automatic sprinkler system in accordance with National Fire Protection Association (NFPA) Standard 25 and NFPA 101 2012. Findings include:1. Sunrise A North Canopy “No information placard is posted listing the solution of the system and how many gallons of antifreeze system is holding” - Mountain View North Women’s hydraulic name plate. “Appears to be missing”2. Visual no hydro calc plate seen
3. Last test for antifreeze testing was 2024Maintenance has a vendor coming out on 3/3/26 to complete how many gallons the antifreeze system is holding and complete the antifreeze testing. The facility is submitting for a time limit waiver for the hydro calc plate to either get the as builds or hire and engineer. Monitoring: Maintenance will confirm that the vendor sends reports and documentation and will maintain said documentation. In compliance on: 4/20/2026
0353Sprinkler System - Maintenance and Testing▼
Findings
Based on observations and interviews, it was determined that the facility failed to meet the protection requirements in accordance with NFPA 101, 25, and 13. Findings Include:IT room in facility lounge sprinkler piping is showing from ceilingSunrise B nurses station sprinkler/escutcheon head not flush with ceiling Quick response sprinkler heads from 1999, 1988 and 1984 - 20 years for quick response and 50 years for standard | Need sample testing completed or replaced Cooler and freezer sprinkler heads need replacement | Existing is from 2016Regulatory Reference:NFPA 25 5.2.1.1.2 Any sprinkler that shows signs of any of the following shall be replaced: (1) Leakage, (2) Corrosion, (3) Physical damage, (4) Loss of fluid in the glass bulb heat responsive element, (5)* Loading (6) Painting unless painted by the sprinkler manufacturer. NFPA 25 5.2.2.2 Sprinkler piping shall not be subjected to external loads by materials either resting on the pipe or hung from the pipe. 5.3.1.1* Where required by this section, sample sprinklers shall be submitted to a recognized testing laboratory acceptable to the authority having jurisdiction for field service testing. 5.3.1.1.1 Where sprinklers have been in service for 50 years, they shall be replaced or representative samples from one or more sample areas shall be tested. 5.3.1.1.1.3* Sprinklers manufactured using fast-response elements that have been in service for 20 years shall be replaced, or representative samples shall be tested and then retested at 10-year intervals. 5.3.1.1.1.6* Dry sprinklers that have been in service for 10 years shall be replaced or representative samples shall be tested and then retested at 10-year intervals. 5.3.1.1.2* Where sprinklers are subjected to harsh environments, including corrosive atmospheres and corrosive water supplies, on a 5-year basis, either sprinklers shall be replaced or representative sprinkler samples shall be tested. This deficiency has the potential to affect all smoke compartments within the facility, and all residents, visitors, and staff. The deficiency was discussed with the life and safety maintenance resource advisor and the maintenance director during the survey exit conference.
Plan of correction · submitted by the facility
K353Sprinkler System – Maintenance and TestingResident Specific: No residents Identified but could affect all residents, staff and visitors within the facility. Identification of others: Potential to affect all occupants, who might include staff, residents and visitors. System and Measures: Based on observations and interviews, it was determined that the facility failed to meet the protection requirements in accordance with NFPA 101, 25, and 13. Findings Include:1. IT room in facility lounge sprinkler piping is showing from ceiling
2. Sunrise B nurses station sprinkler/escutcheon head not flush with ceiling
3. Quick response sprinkler heads from 1999, 1988 and 1984 - 20 years for quick response and 50 years for standard | Need sample testing completed or replaced
4. Cooler and freezer sprinkler heads need replacement | Existing is from 2016The facility has scheduled a vendor to complete repairs on 3/6/2026 for the piping in the IT room and to complete the sample testing. The Cooler and freezer sprinkler heads will be replaced before the 10-year expiration year. The current heads are dated 2016. We will get a quote to get them replaced before the 10-year expiration. Monitoring: Maintenance will confirm that the vendor sends reports and documentation and will maintain said documentation. Maintenance will also do visual checks of the facilities escutcheon to maintain compliance. In compliance on: 4/20/2026
0374Subdivision of Building Spaces - Smoke Barrie▼
Findings
Based on observation and staff interviews, it was determined that the facility failed to maintain fire barriers and fire doors in accordance with NFPA 101 Chapter 19, 8 and NFPA 80. Findings include: Fire/smoke doors with no rating labels found throughout Fire/smoke doors and frames rating labels painted over to dining room and by nurses station Not rated frame and doors by room 411 not known without plans whether fire rated assembly Regulatory Reference: NFPA 101 8.3.3.2* Fire protection ratings for products required to comply with 8.3.3 shall be as determined and reported by a nationally recognized testing agency in accordance with NFPA 252, Standard Methods of Fire Tests of Door Assemblies; ANSI/UL 10B, Standard for Fire Tests of Door Assemblies; ANSI/UL 10C, Standard for Positive Pressure Fire Tests of Door Assemblies; NFPA 257, Standard on Fire Test for Window and Glass Block Assemblies; or ANSI/UL 9, Standard for Fire Tests of Window Assemblies. NFPA 101 8.3.3.2.3* Labels on fire door assemblies shall be maintained in a legible condition. NFPA 101 8.3.3.4 Floor fire door assemblies shall be tested in accordance with NFPA 288, Standard Methods of Fire Tests of Floor Fire Door Assemblies Installed Horizontally in Fire Resistance–Rated Floor Systems, and shall achieve a fire resistance rating not less than the assembly being penetrated. Floor fire door assemblies shall be listed and labeled. This deficiency has the potential to affect approximately 20 residents within the facility, and visitors, and staff. The deficiency was discussed with the life and safety maintenance resource advisor and the maintenance director during the survey exit conference.
Plan of correction · submitted by the facility
K374Subdivision of Building Spaces – Smoke BarriersResident Specific: No residents Identified but could affect all residents, staff and visitors within the facility. Identification of others: Potential to affect all occupants, who might include staff, residents and visitors. System and Measures: Based on observation and staff interviews, it was determined that the facility failed to maintain fire barriers and fire doors in accordance with NFPA 101 Chapter 19, 8 and NFPA 80. Findings include:1. Fire/smoke doors with no rating labels found throughout
2. Fire/smoke doors and frames rating labels painted over to dining room and by nurses’ station
3. Not rated frame and doors by room 411 not known without plans whether fire rated assemblyThe building is working with a vendor to get door ratings and labels for the doors and the frames in question. The maintenance team has removed the paint from the current doors where the labels were painted over. The facility is asking for a time-limit waiver due to not being able to get the building plans to confirm needed ratings throughout the facility. Monitoring: Maintenance will make sure that door rating labels do not get painted and will continue to work with our vendors to maintain compliance with Life Safety codes. In compliance on: 4/20/2026
0500Building Services - Other▼
Findings
Based on observations and staff interviews, it was determined that the facility failed to maintain appliances according to NFPA 70. Findings include: Nurses station in memory care fridges plugged into power strips Regulatory Reference:Flexible cords and cables in accordance with Chapter 4 of NFPA 70, Section 400.8(1), in part, flexible cords and cables shall not be used as a substitute for the fixed wiring of a structure. Furthermore, Health Care Facilities Code section 10.2.3.6 (2), "The sum of the ampacity of all appliances connected to the outlets does not exceed 75 percent of the ampacity of the flexible cord supplying the outlets." This deficiency has the potential to affect approximately 20 residents within the facility, and visitors, and staff. The deficiency was discussed with the life and safety maintenance resource advisor and the maintenance director during the survey exit conference.
Plan of correction · submitted by the facility
K500Building Services - otherResident Specific: No residents Identified but could affect all residents, staff and visitors within the facility. Identification of others: Potential to affect all occupants, who might include staff, residents and visitors. System and Measures: Maintenance removed fridge from power strip and plugged directly into the wall outlet. An education was provided on 2/11/26 to the Maintenance Director, Executive Director and the Maintenance Assistant on the proper use of UL rated power strips in the facility. Monitoring: Maintenance will audit the fridge and the how it is plugged in for 4 weeks. In compliance on: 3/11/26
0521HVAC▼
Findings
Based on ITM record review, observation, and staff interview, the facility failed to maintain the heating, ventilation, and air conditioning (HVAC) system in accordance with the requirements of Life Safety Code NFPA 101 (2012), NFPA 90A (2011), NFPA 80 (2010) and referenced standards. The facility director and regional director of plant operations were present throughout the survey. Findings Include:Documentation of expired K521 waiver during documentation review The facility utilizes evaporative (“swamp”) coolers to provide cooling to resident care areas. Observations confirmed that resident exit access corridors are being used to convey air throughout the facility. The corridors and resident rooms lacked dedicated, ducted HVAC systems. Regulatory Reference: NFPA 101 (2012) § 9.2.1 – Air-Conditioning, Heating, Ventilating Ductwork, and Related Equipment – Air-conditioning, heating, ventilating ductwork, and related equipment shall be in accordance with NFPA 90A, Standard for the Installation of Air-Conditioning and Ventilating Systems, or NFPA 90B, Standard for the Installation of Warm Air Heating and Air-Conditioning Systems, as applicable, unless such installations are approved existing installations, which shall be permitted to be continued in service. NFPA 99 (2012), § 9.3.5 – Ductwork – Heating, cooling, ventilation and process systems serving spaces or providing health care functions covered by this code shall utilize ductwork systems complying with NFPA 90A, Standard for the Installation of Air-Conditioning and Ventilating Systems, or applicable mechanical codes. NFPA 90A (2012), Section 4.3.12.1 – Egress corridors in health care, detention and correctional, and residential occupancies shall not be used as a portion of a supply, return, or exhaust air system serving adjoining areas unless otherwise permitted by 4.3.12.3.1 through 4.3.12.1.3.4. This deficiency has the potential to affect all smoke compartments within the facility, and all residents, visitors, and staff. The deficiency was discussed with the life and safety maintenance resource advisor and the maintenance director during the survey exit conference.
Plan of correction · submitted by the facility
K521HVACResident Specific: No residents Identified but could affect all residents, staff and visitors within the facility. Identification of others: Potential to affect all occupants, who might include staff, residents and visitors. System and Measures: Based on ITM record review, observation, and staff interview, the facility failed to maintain the heating, ventilation, and air conditioning (HVAC) system in accordance with the requirements of Life Safety Code NFPA 101 (2012), NFPA 90A (2011), NFPA 80 (2010) and referenced standards. The facility director and regional director of plant operations were present throughout the survey. Findings Include:1. Documentation of expired K521 waiver during documentation review
2. The facility utilizes evaporative (“swamp”) coolers to provide cooling to resident care areas. Observations confirmed that resident exit access corridors are being used to convey air throughout the facility. The corridors and resident rooms lacked dedicated, ducted HVAC systems. The facility is requesting a time limit waiver for K-521Monitoring: Maintenance will maintain the waiver in their records once its received. In compliance on: 4/20/2026
0741Smoking Regulations▼
Findings
Based on observation and staff interview, it was determined that the facility did not have the proper receptacles in place in the allowed smoking areas in accordance with NFPA 101. These items were discussed during the survey walkthrough. Findings include: No metal can by door by kitchen for smoking area Regulatory Reference:NFPA 101 201219.7.4* Smoking regulations shall be adopted and shall include not less than the following provisions:(1)Smoking shall be prohibited in any room, ward, or individual enclosed space where flammable liquids, combustible gases, or oxygen is used or stored and in any other hazardous location, and such areas shall be posted with signs that read NO SMOKING or shall be posted with the international symbol for no smoking.(2)In health care occupancies where smoking is prohibited and signs are prominently placed at all major entrances, secondary signs with language that prohibits smoking shall not be required.(3)Smoking by patients classified as not responsible shall be prohibited.(4)The requirement of 19.7.4(3) shall not apply where the patient is under direct supervision.(5)Ashtrays of noncombustible material and safe design shall be provided in all areas where smoking is permitted.(6)Metal containers with self-closing cover devices into which ashtrays can be emptied shall be readily available to all areas where smoking is permitted. This deficiency has the potential to affect approximately 20 residents within the facility, and visitors, and staff. The deficiency was discussed with the life and safety maintenance resource advisor and the maintenance director during the survey exit conference.
Plan of correction · submitted by the facility
K741Smoking RegulationsResident Specific: No residents Identified but could affect all residents, staff and visitors within the facility. Identification of others: Potential to affect all occupants, who might include staff, residents and visitors. System and Measures: Maintenance purchased a red metal can and installed it at the smoking area. Maintenance will maintain the smoking area weekly. Monitoring: Maintenance will make sure the can is in the proper location weekly. In compliance on: 2/25/26
0918Electrical Systems - Essential Electric Syste▼
Findings
Based on observation and record review during the survey, it was determined that the facility failed to maintain the back-up emergency generator in accordance with National Fire Protection Association (NFPA) Standard 110. This was evidenced by the following: Findings include: Facility needs to protect natural gas valve for generator Regulatory Reference:NFPA 1108.1.1 The routine Maintenance and operational testing program shall be based on all of the following: Manufacturers recommendationsInstruction manualsMinimum requirements of this chapterThe authority having jurisdiction 7.9.7* Where the gas supply is connected to the building gas supply system, it shall be connected on the supply side of the main gas shutoff valve marked as supplying and emergency generator. A.?7.9.7 Valving for natural gas–fueled prime movers should be configured so that the gas supply to the prime mover cannot be inadvertently or intentionally shut off by anyone other than qualified personnel such as the gas supplier. If valves are placed in an isolated area, a secure area or locking the valve(s) open is recommended. This deficiency has the potential to affect all smoke compartments within the facility, and all residents, visitors, and staff. The deficiency was discussed with the life and safety maintenance resource advisor and the maintenance director during the survey exit conference.
Plan of correction · submitted by the facility
K918Electrical Systems – Essential Electrical SystemResident Specific: No residents Identified but could affect all residents, staff and visitors within the facility. Identification of others: Potential to affect all occupants, who might include staff, residents and visitors. System and Measures: Based on observation and record review during the survey, it was determined that the facility failed to maintain the back-up emergency generator in accordance with National Fire Protection Association (NFPA) Standard 110. This was evidenced by the following:Findings include:1. Facility needs to protect natural gas valve for generatorMaintenance has ordered a lock device for the valve and will install it once it arrives from the vendor. Monitoring: Maintenance will check the lock when they do the weekly visual of the generator. In compliance on: 3/6/26
0923Gas Equipment - Cylinder and Container Storag▼
Findings
Based on observation during the course of the survey it was determined the facility failed to maintain a hazardous area in accordance with NFPA 99. This was evidenced by the following: Findings include: Oxygen rooms cylinders need to be labeled/separated by empty and fullRegulatory Reference:NFPA 99: 11.6.5.2 If empty and full cylinders are stored within the same enclosure, empty cylinders shall be segregated from full cylinders. This deficiency has the potential to affect approximately 10 residents within the facility, and visitors, and staff. The deficiency was discussed with the life and safety maintenance resource advisor and the maintenance director during the survey exit conference.
Plan of correction · submitted by the facility
K923Gas Equipment – Cylinder and Container StorageResident Specific: No residents Identified but could affect all residents, staff and visitors within the facility. Identification of others: Potential to affect all occupants, who might include staff, residents and visitors. System and Measures: Based on observation during the course of the survey it was determined the facility failed to maintain a hazardous area in accordance with NFPA 99. This was evidenced by the following:Findings include:1. Oxygen rooms cylinders need to be labeled/separated by empty and fullMaintenance added noncombustible signage to the oxygen room. Monitoring: Maintenance installed permanent signage and will replace if room is ever painted. In compliance on: 2/10/26
0927Gas Equipment - Transfilling Cylinders▼
Findings
Based on observation and interview, the facility’s transfill locations were not maintained in accordance with NFPA 99 and NFPA 55. This deficiency was identified to staff during the survey walk-through. Findings include: Oxygen transfer room no ventilation 12” from floor | Ventilation in ceiling must be maintained as well Regulatory Reference:NFPA 9911.5.2.3.1 Transfilling to liquid oxygen base reservoir containers or to liquid oxygen portable containers over 344.74 kPa (50 psi) shall include the following:(1) A designated area separated from any portion of a facility wherein patients are housed, examined, or treated by a fire barrier of 1 hour fire-resistive construction.(2) The area is mechanically ventilated, is sprinklered, and has ceramic or concrete flooring.(3) The area is posted with signs indicating that transfilling is occurring and that smoking in the immediate area is not permitted.(4) The individual transfilling the container(s) has been properly trained in the transfilling procedures. 9.3.7.5.3 Mechanical Ventilation. 9.3.7.5.3.1 Mechanical exhaust to maintain a negative pressure in the space shall be provided continuously, unless an alternative design is approved by the authority having jurisdiction. 9.3.7.5.3.2 Mechanical exhaust shall be at a rate of 1 L/sec of airflow for each 300 L (1 cfm per 5 ft3 of fluid) designed to be stored in the space and not less than 24 L/sec (50 cfm) nor more than 235 L/sec (500 cfm). 9.3.7.5.3.3 Mechanical exhaust inlets shall be unobstructed and shall draw air from within 300 mm (1 ft) of the floor and adjacent to the cylinder or containers. 9.3.7.5.3.4 Mechanical exhaust air fans shall be supplied with electrical power from the essential electrical system. NFPA 556.15.7 Inlets to the Exhaust System. 6.15.7.1 The exhaust ventilation system design shall take into account the density of the potential gases released. 6.15.7.2 For gases that are heavier than air, exhaust shall be taken from a point within 12 in. (304.8 mm) of the floor. 6.15.7.3 For gases that are lighter than air, exhaust shall be taken from a point within 12 in. (304.8 mm) of the ceiling. This deficiency has the potential to affect approximately 10 residents within the facility, and visitors, and staff. The deficiency was discussed with the life and safety maintenance resource advisor and the maintenance director during the survey exit conference.
Plan of correction · submitted by the facility
K923Gas Equipment – transfilling CylindersResident Specific: No residents Identified but could affect all residents, staff and visitors within the facility. Identification of others: Potential to affect all occupants, who might include staff, residents and visitors. System and Measures: Based on observation and interview, the facility’s trans fill locations were not maintained in accordance with NFPA 99 and NFPA 55. This deficiency was identified to staff during the survey walk-through. Findings include:1. Oxygen transfer room no ventilation 12” from floor | Ventilation in ceiling must be maintained as well. Maintenance will complete the low vent installation per the Life Safety codes. Monitoring: Maintenance will do monthly checks to monitor the vent and that it is working properly. In compliance on: 3/27/26
1/15/2026Licensure Complaint, Re-Licensure Survey · ID 1E05E1-H1No deficiencies▼
0000Initial CommentsSurveyor note▼
Findings
A licensure survey with #CO2708747 was completed on 1/11/26 to 1/15/26. No deficiencies were cited.
Plan of correction
The state did not require a plan of correction for this citation.
9999Final ObservationsSurveyor note▼
Findings
THIS PORTION OF THE REPORT IS FOR INFORMATIONAL PURPOSES ONLY.No response is necessary. The residence was advised it must review and maintain the following processes in accordance with existing program regulations found at 6 CCR 1011-1, Chapter 5. 7.5 BEHAVIORAL HEALTH CAREA) For residents with behavioral health issues, the facility shall:1) Note the behavioral issue and evaluate it in the resident’s assessment;2) Develop and implement an individualized treatment plan designed to address the behavioral health issue;3) Obtain a mental health evaluation in appropriate cases; and,4) Evaluate the resident's progress and revise the plan, both as needed and whenever there is a change in the resident’s behavioral condition. B) For residents receiving medication for behavior modification, the facility shall indicate in the health information record positive and/or negative effects of the medication and what alternatives to the medication were considered. 9.10 D. At least every two hours residents with safety devices shall be observed and such observation shall be documented. 22.2 E Each resident room shall be equipped with a communication system to allow residents to call for staff assistance. The system shall be capable of activation from the resident’s bed, with emergency activation from the toilet room, and each tub and shower. The system shall notify staff of a request for assistance via audible, visual or electronic means. 23.2 There shall be a designated team to evaluate placement of a resident in a secure environment. The team shall include, at a minimum, the director of nursing or designee, a social services staff member, the administrator or designee and an individual (with mental health or social work training as appropriate to the needs of the residents) who is not a facility staff member. 23.4 A 4) The resident or resident representative has given informed, written consent.
Plan of correction
The state did not require a plan of correction for this citation.
1/15/2026Complaint, Recertification Survey · ID 1E05DD-H16 deficiencies▼
0000Initial CommentsSurveyor note2 building records▼
Findings · record 1 of 2
A recertification survey with complaints #CO2653738, #CO2664595, #CO2670211, Incident #2687603 and Incident #2694611 was conducted on 1/11/26 to 1/15/26. Six deficiencies were cited.
Findings · record 2 of 2
An Emergency Preparedness survey was conducted from 1/11/26 to 1/15/26. No deficiencies were cited.
Plan of correction
The state did not require a plan of correction for this citation.
0605Right to be Free from Chemical Restraints▼
Findings
Based on record review and interviews, the facility failed to ensure one (#1) of five residents reviewed for psychotropic medications out of 37 sample residents were as free from unnecessary medications as possible. Specifically, the facility failed to:-Ensure Resident #1 had behavior monitoring in place for antipsychotic use; and,-Ensure consents were obtained prior to administration of psychotropic medications. Findings include:I. Facility policy and procedureThe Chemical Restraints and Psychotropic Medication Management policy and procedure, revised April 2025, was provided by the regional consultant on 1/15/26 at 2:42 p.m. It read in pertinent part, “It is the policy of this facility to ensure that residents are free from chemical restraints imposed for purposes of discipline or convenience or that are not required to treat a specific condition as diagnosed and documented in the clinical record. Psychotropic medications shall not be administered for the purpose of discipline or convenience.“Residents who use psychotropic drugs receive gradual dose reductions (GDR), and behavioral interventions, unless clinically contraindicated, in an effort to discontinue these drugs.“The licensed nurse shall review the classification of the drug, the appropriateness of the diagnosis, its indication, behavior monitors and related adverse side effects prior to verification of admission orders with the attending physician.“The social services director (SSD) and/or nursing designee will be responsible for initiating the residents’ individualized, person-centered psychosocial plan of care, based on their comprehensive initial admission assessment.“Upon initial comprehensive assessment, the SSD designee shall review new admissions for any psychiatric, mood or behavior disorders, mental and psychosocial difficulties, and/or physician's orders for psychotropic medications. The facility's interdisciplinary team (IDT) will review to ensure: psychotropic medication was prescribed to treat a specific diagnosed condition, as documented in the clinical record; not in excessive dosage; behavior is not related to delirium or other reversible conditions; monitoring for adverse consequences and effectiveness of medications are in place; PRN medications are within guidelines; informed consent was obtained prior to medication use; review of plan of care shows individualized, person-centered care approaches to manage behavior with non-pharmacological interventions; attempt/consider a GDR, if appropriate.” II. Resident #1A. Resident statusResident #1, age 76, was admitted on 12/22/25. According to the January 2026 computerized physician orders (CPO), diagnoses included pneumonia, chronic obstructive pulmonary disease and dementia. The 12/26/25 minimum data set (MDS) assessment revealed the resident was cognitively intact with a brief interview for mental status (BIMS) score of 13 out of 15. The MDS assessment revealed Resident #1 was dependent on staff for lower body dressing and needed partial assistance for upper body dressing and needed substantial assistance for toileting and bathing and was independent with eating. The MDS assessment further revealed Resident #1 did not have any behaviors of psychosis, verbal or physical aggression, or other behavioral symptoms such as pacing, exit seeking, rejection of care or sexual inappropriate behavior. The MDS assessment revealed Resident #1 had mild depression with a score of eight out of 27. The MDS assessment revealed Resident #1 received antidepressant, antianxiety and antipsychotic medications. B. Record reviewReview of Resident #1’s January 2026 CPO revealed the following physician’s orders: Citalopram Hydrobromide (Celexa, an antidepressant medication) 20 milligram (mg) tablet. Give one tablet by mouth one time a day for depression, ordered 12/22/25. Clonazepam (an antianxiety medication) 1 mg tablet. Give one tablet by mouth in the morning for anxiety, ordered 12/22/25. Quetiapine Fumarate (Seroquel, an antipsychotic medication) 100 mg tablet. Give 100 mg by mouth at bedtime for dementia, ordered 12/22/25. Review of Resident #1’s electronic medical record (EMR) revealed a psychoactive medication evaluation, dated 12/23/25 for Seroquel 100 mg. The diagnosis listed for the medication was dementia. -The evaluation did not document any behaviors for Resident #1. Resident #1’s potential for a psychosocial well-being problem care plan, referring to the resident’s mild depression, initiated 12/22/25 and revised 1/2/26, documented social services offered mental health counseling services which Resident #1 accepted. The interventions included allowing time for the resident to answer questions and to verbalize feelings, perceptions, and fears, providing opportunities for family to participate in care, and when conflict arose, removing the resident to a calm safe environment and allowing the resident to vent/share feelings. -The care plan failed to document specific target behaviors to monitor for Resident #1 in order to justify the use of the resident’s psychotropic and antipsychotic medications. Review of Resident #1’s December 2025 and January 2026 medication administration records (MAR) revealed there was no documentation for mood or behavior tracking. Review of Resident #1’s December 2025 and January 2026 MARs documented tracking of sleep and side effects for the resident’s antidepressant medication; however, the MARs failed to reveal side effect tracking for the resident’s antipsychotic and antianxiety medications. The pharmacy consultation report, dated 1/8/26, recommended for the facility to add behavior and side effect tracking to Resident #1’s MAR for the medications clonazepam, citalopram and Seroquel. -Review of Resident #1’s EMR did not reveal any documentation to indicate the facility obtained consent to administer the resident’s psychotropic medications. III. Staff interviewsRegistered nurse (RN) #5 was interviewed on 1/15/26 at 10:21 a.m. RN #5 said Resident #1 was on Seroquel for dementia and clonazepam for anxiety. She said the facility was monitoring the resident’s hours of sleep for her antidepressant. She said Resident #1 did not have any behaviors. Director of nursing (DON) #1 was interviewed on 1/15/26 at 1:07 p.m. DON #1 said staff knew what resident behaviors to monitor for because the behavior monitoring was on the behavior tracking care plan. She said it was then documented on either the treatment administration record (TAR) or the MAR. She said once the facility was able to determine triggers and non-pharmacological interventions through observations and interviews, all of the information would be documented on the resident’s care plan. She said if a resident had a behavior, the interventions for the behavior were documented on the care plan and the Kardex (a reference tool that summarizes vital resident data). She said interventions that were used during a behavioral moment and if the intervention was effective or not were documented on the TAR or the MAR. She said for Resident #1, the facility was monitoring the resident’s hours of sleep for a sleep aid, and she could not find a specific behavior for the resident’s antipsychotic medication. She said the facility should have triggered antipsychotic behavior. She said the facility should have documentation of the psychotropic medication consents but sometimes, they did not upload them until they could get the physical signature. -However, during the survey process, the consents were requested and the facility did not provide documentation of them.
Plan of correction · submitted by the facility
Resident Specific: The facility failed to ensure one (#1) of five residents reviewed for psychotropic medications out of 37 sample residents were as free from unnecessary medications as possible. Facility failed to ensure Resident #1 had behavior monitoring in place for antipsychotic use and failed to ensure consents were obtained prior to administration of psychotropic medications. Facility updated behavior monitoring for resident #1 and completed consent form per facility protocol. Identification of Other Residents:An audit was completed by DON (director of nursing)/SSD (social services director) to ensure all residents with behaviors had monitoring in place along with consents for the use of psychotropics. No other residents identified or affected. Systems and Measures: Education initiated to DON and SSD to ensure all psychotropic medications ordered have a consent form completed before administration takes place. Nurse managers were educated on ensuring that once behaviors are observed/noted that resident(s) have behavior tracking in place. Monitoring: The Director of Nursing or designee will complete audits to ensure behavior tracking and consent forms are in place 3 times weekly for 90 days. Audit form will include date, resident name, name of the psychotropic, if behavior tracking is in place, if the consent form is completed before administration of the medication and if the information is care planned. Monitoring will be included in monthly QAPI.
0657Care Plan Timing and Revision▼
Findings
Based on record review and interviews, the facility failed to ensure the comprehensive care plan was reviewed and revised timely to include the instructions needed to provide effective and personalized care for one (#9) of three residents out of 37 sample residents. Specifically, the facility failed to revise Resident #9’s care plan to address catheter care interventions for the prevention of recurrent urinary tract infections (UTI). Findings include: I. Facility policy and procedureThe Care Planning policy and procedure, revised March 2020, was provided by the regional consultant on 1/15/26 at 2:42 p.m. It read in pertinent part,“It is the policy of this facility that the interdisciplinary team (IDT) shall develop a comprehensive care plan for each resident. “Will complete an initial care plan within 48 hours of admission.“A comprehensive care plan is developed within seven (7) days of completion of the Resident Minimum Data Set (MDS) Assessment.”The Catheter Care policy and procedure, revised April 2021, was provided by the regional consultant on 1/15/26 at 2:42 p.m. It read in pertinent part, “It is the policy of this facility to reduce the risk of catheter- associated urinary tract infection.“Use standard precautions when handling or manipulating the drainage system. Maintain clean technique when handling or manipulating catheter, tubing, or drainage bag. Empty drainage bag every shift and as needed using a graduated cylinder to measure if indicated. “Certified nurse aides (CNA) may also perform catheter care and notify the nurse.”II. Resident #9A. Resident statusResident #9, age 77, was admitted on 9/15/23. According to the January 2026 computerized physician orders (CPO), diagnoses included unspecified dementia, Parkinson’s disease (neurological disorder affecting movement), benign prostatic hyperplasia with lower urinary tract symptoms (enlarged prostate causing urinary issues), unspecified urethral stricture, male, unspecified site ( narrowing of the male urethra) and bladder neck obstruction (blockage at the base of the bladder). The 12/5/25 minimum data set (MDS) assessment revealed Resident #9 had severe cognitive impairments with a brief interview for mental status (BIMS) score of zero out of 15. Resident #9 required partial to moderate assistance with oral hygiene, toileting hygiene, personal hygiene, and upper body dressing. Resident #9 was dependent on staff for lower-body dressing and needed substantial to maximal assistance with bathing. The assessment revealed Resident #9 had an indwelling catheter. B. Record reviewThe methenamine hippurate (non-antibiotic prescription antiseptic used for preventing UTI) care plan, revised 12/16/24, revealed the goal was for Resident #9 to be free from infection (revised 9/24/25 with a target date of 3/5/26). Interventions (revised 12/16/24) included educating the resident, family members and caregivers regarding the importance of handwashing, using soap and water and drying hands using disposable towels, encouraging fluid intakes and enhanced barrier precautions during close contact care, monitoring the resident for signs and symptoms of an active infection, obtaining and monitoring laboratory/diagnostic work as ordered and reporting results to the physician. The suprapubic catheter for obstructive and reflux uropathy care plan, revised 12/1/25, revealed the goal for Resident #9 was for the resident to show no signs or symptoms of urinary infection and remain free from catheter-related trauma (revised 9/24/25). Interventions included positioning the resident’s catheter bag and tubing below the level of the bladder, changing catheter bag and tubing as ordered, discussing with resident/representative the risks and benefits of the use of a catheter, removal of the catheter when criteria for use was no longer present and the right to decline the use of the catheter, providing catheter care every shift and as needed, measuring urinary output, monitoring for signs and symptoms of discomfort on urination and frequency, urology appointments as needed and using enhanced barrier precautions. The 3/21/25 at 2:33 p.m. alert note documented Resident #9 required cues to encourage him from pulling on his catheter. The 10/16/25 at 2:40 p.m. nursing note documented Resident #9 was encouraged to not tamper with the catheter tubing. The 11/30/25 at 11:23 a.m. therapy note documented Resident #9 was being seen by speech therapy. Per IDT discussion, speech therapy would work on educating Resident #9 on catheter hygiene. The 12/1/25 at 11:14 a.m. IDT fall committee note documented part of the root cause analysis for the resident’s fall was due to Resident #9’s UTI. It was documented Resident #9 would often unhook and touch his catheter frequently throughout the day due to his impaired cognition and the resident did not recall staff education. The note further documented speech therapy would attempt to work on educating Resident #9 on appropriate catheter hygiene and care. The 12/2/25 at 3:30 p.m. IDT note documented barriers to Resident #9's UTI treatment were Resident #9’s cognition and his frequent touching of the catheter tubing and his skin without proper hand hygiene and catheter care. The note further documented occupational therapy had done an evaluation and speech therapy was there to help with education and maintenance of hygiene and catheter care needs. The 12/4/25 at 11:49 a.m. nurse practitioner (NP) note documented Resident #9 was being seen for recurrent UTI and catheter pain. The note documented Resident #9 manipulated his catheter tubing. The 12/5/25 at 10:10 a.m. the condition follow-up note documented staff continued to assist with catheter care and reminding Resident #9 not to touch the catheter tubing and bag when witnessed. On 12/11/25 continued education was given to the staff for catheter care for Resident #9. The education provided was to continue to encourage Resident #9 to not touch his suprapubic catheter, continue to assist Resident #9 with handwashing, engage Resident #9 in activities, offer snacks to keep the resident’s attention off of his catheter, encourage fluids and empty urination bag timely to prevent Resident #9 from trying to complete the task on his own.-However, Resident #9’s UTI and catheter care plans failed to document the new interventions put in place to help prevent Resident #9 from touching his catheter tubing, leading to the resident’s frequent UTIs (see care plans above). III. Staff interviewsCNA #3 was interviewed on 1/13/26 at 2:33 p.m. CNA #3 said Resident #9 had a catheter leg bag and CNAs would do catheter care for Resident #9 at least once every shift. She said CNAs would use alcohol swabs and clean the catheter away from his abdomen, because he had a suprapubic catheter. CNA #4 was interviewed on 1/13/26 at 3:46 p.m. CNA #4 said CNAs would do Resident #9’s catheter care once a shift. She said they would use the peri care wipes to clean his tubing away from his abdomen. Registered nurse (RN) #2 was interviewed on 1/14/26 at 7:39 a.m. RN #2 said the nurses normally did the residents’ catheter care. She said Resident #9 had chronic extended-spectrum beta-lactamase (ESBL), specifically E.coli. She said she normally did Resident #9’s catheter care and the CNAs would do it as needed on top of what she did. The infection preventionist (IP) and director of nursing (DON) #1 were interviewed together on 1/15/25 at 10:10 a.m. The IP said she was responsible for monitoring and tracking infection trends in the facility. The IP said every resident who had an indwelling urinary catheter would also have a care plan for catheter care to prevent urinary tract infections. She said Resident #9 should have had a care plan with interventions for the nursing staff to utilize in order to prevent infections. DON #1 said all nursing staff were trained to do catheter care and used an alcohol wipe for cleaning. She said catheter care should be done at a minimum of once per 12 hour shift, or asneeded. DON #1 said Resident #9 had chronic urinary tract infections because he had dementia and he continuously put his hands down his pants and touched his catheter. She said the facility encouraged staff to keep the resident’s catheter bag empty, make sure Resident #9’s hands were washed and clean and distract Resident #9 from putting his hands down his pants. DON #1 said all of these interventions were known by the nursing staff due to the education that was given to them. - However, the interventions were not updated on Resident #9’s care plan (see care plans above).
Plan of correction · submitted by the facility
Resident Specific: The facility failed to ensure the comprehensive care plan was reviewed and revised timely to include the instructions needed to provide effective and personalized care for one (#9) of three residents out of 37 sample residents. The facility failed to revise Resident #9’s care plan to address catheter care interventions for the prevention of recurrent urinary tract infections (UTI). Upon notification on 1/15/26 the DON updated resident #9’s care plan to address catheter care interventions. Identification of Other Residents: On 1/15/26 DON/IP (infection preventionist) audited resident care plans to ensure resident personalized care plans were in place. 2 residents found to be missing item(s) and corrected on this day (01/15/26). Systems and Measures: Education on 1/15/26 was provided to IDT (interdisciplinary team) to ensure morning meeting includes care plan updates. This will ensure interventions/items are not being missed. In addition, if new interventions are put into place they should be included in the resident care plan as soon as possible. Staff on the floor will be educated on the interventions during morning huddle. Monitoring: The Director of Nursing or designee will complete audits to ensure all resident personalized care plans are in place and updated timely. This audit will take place 3 times weekly for 90 days. Audit form will include date, resident name, what the new intervention is, if it was added to the care plan timely and a space for notes/education. Monitoring will be included in monthly QAPI.
0686Treatment/Svcs to Prevent/Heal Pressure Ulcer▼
Findings
Based on observations, record review and interviews, the facility failed to ensure two (#78 and #70) of three residents reviewed for pressure injuries out of 37 sample residents received care consistent with professional standards of practice to prevent pressure ulcers from developing or worsening. Specifically the facility failed to:-Ensure staff consistently offloaded Resident #78’s heels; and, -Ensure staff consistently provided wound care to Resident #78 and Resident #70 in a timely manner, per physician’s orders. Findings include:I. Professional reference According to the National Pressure Injury Advisory Panel, European Pressure Injury Advisory Panel and Pan Pacific Pressure Injury Alliance Prevention and Treatment of Pressure Injuries: Clinical Practice Guideline, third edition, Emily Haesler (Ed.), EPUAP/NPIAP/PPPIA (2019) retrieved on 1/20/26 from https://www.internationalguidelines.com/guideline, "Pressure ulcer classification is as follows:"Category/Stage 1: Nonblanchable Erythema (discoloration of the skin that did not turn white when pressed, early sign of tissue damage)Intact skin with nonblanchable redness of a localized area usually over a bony prominence. Darkly pigmented skin may not have visible blanching; its color may differ from the surrounding area. The area may be painful, firm, soft, warmer or cooler as compared to adjacent tissue. Category/Stage 1 may be difficult to detect in individuals with dark skin tones. May indicate 'at risk' individuals (a heralding sign of risk)."Category/Stage 2: Partial Thickness Skin LossPartial thickness loss of dermis presenting as a shallow open ulcer with a red pink wound bed, without slough. May also present as an intact or open/ruptured serum filled blister. Presents as a shiny or dry shallow ulcer without slough or bruising. This Category/Stage should not be used to describe skin tears, tape burns, perineal dermatitis, maceration or excoriation."Category/Stage 3: Full Thickness Skin LossFull thickness tissue loss. Subcutaneous fat may be visible, but bone, tendon or muscle were not exposed. Slough may be present but did not obscure the depth of tissue loss. May include undermining and tunneling. The depth of a Category/ Stage 3 pressure ulcer varies by anatomical location. The bridge of the nose, ear, occiput and malleolus do not have subcutaneous tissue and Category/ Stage 3 ulcers can be shallow. In contrast, areas of significant adiposity can develop extremely deep Category/Stage 3 pressure ulcers. Bone/tendon is not visible or directly palpable."Category/Stage 4: Full Thickness Tissue LossFull thickness tissue loss with exposed bone, tendon or muscle. Slough or eschar may be present on some parts of the wound bed. Often include undermining and tunneling. The depth of a Category/Stage 4 pressure ulcer varies by anatomical location. The bridge of the nose, ear, occiput and malleolus do not have subcutaneous tissue and these ulcers can be shallow. Category/ Stage 4 ulcers can extend into muscle and/ or supporting structures (fascia, tendon or joint capsule) making osteomyelitis possible. Exposed bone/tendon is visible or directly palpable"Unstageable: Depth UnknownFull thickness tissue loss in which the base of the ulcer is covered by slough (yellow, tan, gray, green or brown) and/or eschar (tan, brown or black) in the wound bed. Until enough slough and/or eschar is removed to expose the base of the wound, the true depth, and therefore Category/ Stage, cannot be determined. Stable (dry, adherent, intact without erythema or fluctuance) eschar on the heels serves as 'the body's natural (biological) cover' and should not be removed. "Suspected Deep Tissue Injury: Depth UnknownPurple or maroon localized area of discolored intact skin or blood-filled blister due to damage of underlying soft tissue from pressure and/or shear. The area may be preceded by tissue that is painful, firm, mushy, boggy, warmer or cooler as compared to adjacent tissue. Deep tissue injury may be difficult to detect in individuals with dark skin tones. Evolution may include a thin blister over a dark wound bed. The wound may further evolve and become covered by thin eschar. Evolution may be rapid, exposing additional layers of tissue even with optimal treatment."II. Resident #78A. Resident statusResident #78, age greater than 65, was admitted on 8/16/23 and readmitted on 2/8/24. According to the January 2026 computerized physician orders (CPO), diagnoses included dementia, anxiety, hypothyroidism, pain and insomnia. According to the 12/5/25 minimum data set (MDS) assessment, Resident #78 was cognitively impaired and was not able to complete a mental assessment as indicated with a brief interview for mental status (BIMS) score of zero out of 15. She required substantial/maximal assistance of two staff members for showering/bathing, dressing and transferring. The MDS assessment documented that the resident was at risk of developing pressure ulcers and had an unstageable pressure ulcer on her right heel that was not present upon admission or reentry. B. ObservationsOn 1/14/26 at 9:15 a.m. Resident #78 was lying on her right side in bed. Two foam heel booties were observed in the resident’s closet in her room. The resident was lying on an air mattress and did not have heel protection devices on either of her feet.-However, the resident's care plan indicated to float her heels as tolerated. Additionally, the resident’s care plan was not updated to indicate the resident had an air mattress (see care plan below). On 1/14/26 at 9:20 a.m. Resident #78’s wound care was observed with the assistant director of nursing (ADON) and certified nurse aide (CNA) #6. After the ADON removed the resident’s socks, Resident #78 was noted to have a black necrotic area (dead tissue) on her right heel. There was no wound care dressing covering the resident’s right heel when the ADON removed the resident’s socks. -However, according to the resident’s January 2026 CPO, Resident #78 should have a protective dressing on her right heel (see physician’s orders below). C. Record reviewA skin assessment, dated 1/3/26, documented Resident #78 was admitted without any pressure injuries to her heels measuring a length of 0.5 centimeters (cm) and width of 0.4 cm. The skin assessment indicated the resident’s right heel wound onset date was 11/23/25. Review of Resident #78’s January 2026 CPO revealed the following physician’s orders:Wound care for right heel: Cleanse right heel area, pat dry, apply hydrocolloid dressing. Change once weekly on Fridays and as needed if dislodged, ordered 12/12/25. -However, there was no dressing on Resident #78’s right heel when wound care was performed (see observation above). Encourage resident to offload heels and side to side position while in bed, ordered 7/19/25.-However, Resident #78’s heels were noted to be positioned directly onto her air mattress and not offloaded on 1/14/26 (see observations above). Resident #78's skin integrity care plan, initiated 11/14/24, revealed Resident #78 had potential for pressure ulcer development related to disease process and immobility. Pertinent interventions included floating heels as necessary, encouraging the resident to turn and reposition and providing assistance as needed and administering treatments as ordered and monitoring for effectiveness. -The staff failed to consistently implement the interventions on the care plan for protection of the resident's heels (see observations above). III. Resident #70A. Resident statusResident #70, age greater than 65, was admitted on 5/13/24. According to the January 2026 CPO, diagnoses included hypertension, chronic kidney disease, anxiety, depression and transient ischemic attack. According to the 10/23/25 MDS assessment, Resident #70 was severely cognitively impaired and was not able to complete a mental assessment as indicated with a brief interview for mental status (BIMS) score of zero out of 15. He required substantial/maximal assistance of two staff members for showering/bathing, dressing and transferring. The MDS assessment documented that the resident was at risk of developing pressure ulcers and had an unstageable pressure ulcer that was not present upon admission or reentry. B. ObservationsOn 1/13/26 at 2:03 p.m. Resident #70’s right heel wound care was observed with registered nurse (RN) #6. The wound dressing on the resident’s right heel was dated 1/9/26, indicating wound care had not been provided to the resident for four days. -However, the physician’s orders for wound care instructed the nursing staff to change the wound dressing daily (see physician’s orders below). C. Record review Review of Resident #70’s January 2026 CPO revealed the following physician’s order:Wound care orders to right heel: Cleanse area to right heel, pat dry, cover wound bed with xeroform to fit and cover with bordered gauze daily and as needed, ordered 1/9/26.-However, the resident’s dressing had not been changed since 1/9/26, a four-day period (see observations above). Resident #70’s skin integrity care plan, initiated 11/5/25, revealed the resident had an actual impairment to skin integrity related to a stage 3 ulcer to right heel and an abrasion to left lateral malleolus (ankle bone). Pertinent interventions included administering treatments as ordered, enhanced barrier precautions, pressure reducing mattress and cushion and wound rounds to follow weekly as needed (initiated 11/12/25). IV. Staff interviews. RN #6 was interviewed on 1/13/26 at 2:10 p.m. RN #6 said Resident #70 had a physician’s order for his wound care dressing to be changed every day during the day shift, or as needed. She said the resident’s' dressing on his right heel should have been completed on the prior day shift (1/12/26) by the on-duty nurse. RN #6 said the resident often declined to wear his offloading boots. RN #6 said she typically did not have a problem completing wound care for the residents. She said there were plenty of staff members working during the day to help with wound care dressings if it were needed. CNA #6 was interviewed on 1/14/26 at 9:25 a.m. CNA #6 said Resident #78 was very weak and frail and was currently on hospice services. She said the nursing staff tried to make the resident comfortable by repositioning her and assisting her with eating and bathing hygiene. CNA #6 said the resident had dressings on her body to prevent her from acquiring worsening wounds. She said if she noticed any dressings that were missing, she was instructed to notify the nursing staff. CNA #6 said the resident should have her offloading boots on while in bed because the resident was unable to reposition herself. Director of nursing (DON) #1, the assistant director of nursing (ADON) and the regional consultant were interviewed together on 1/14/26 at 10:43 a.m. The ADON said she was not wound care certified, but worked as the wound care nurse for the facility on a full-time basis Monday through Friday. The ADON said her duties included conducting wound care audits, weekly skin check documentation audits of the nursing staff, completing resident admission documentation and completing weekly rounds with a wound care physician. The ADON said the nursing staff were responsible for completing daily dressing changes and skin assessments for the residents. The ADON said the dressing for Resident #70 should have been completed daily according to the physician's order. The ADON said Resident #78 should have had a dressing applied to her right heel. The ADON said Resident #78’s heels needed to be off loaded in order to prevent the resident’s heel wound from worsening. DON #1 said she would provide staff training regarding adhering to physician’s orders, specifically regarding wound care. DON #1 said the nursing staff would often be extremely busy with other resident care duties. DON #1 said the reason why Resident #70 and Resident #78 did not have timely wound care completed could have been the result of the nurses being extremely busy. DON #1 said it was the nurse’s responsibility to reach out for assistance to the administrative staff to get all nursing duties completed, including wound care. The regional consultant said it would be critically important for the nursing staff to follow the physician’s orders regarding wound care to prevent infections or additional wound development. The regional consultant said Resident #70 was often non-compliant with his wound care dressing, and the facility failed to add this information to the resident’s care plan. The regional consultant said she would update the resident’s care plan today (1/14/26).
Plan of correction · submitted by the facility
Resident Specific: The facility failed to ensure two (#78 and #70) of three residents reviewed for pressure injuries out of 37 sample residents received care consistent with professional standards of practice to prevent pressure ulcers from developing or worsening. The facility failed to ensure staff consistently offloaded Resident #78’s heels and failed to ensure staff consistently provided wound care to Resident #78 and Resident #70 in a timely manner, per physician’s orders. The facility immediately began education (1/14/26) with all the nursing staff regarding timely wound care treatment. The facility also educated nurses and CNA’s (certified nurse aides) on ensuring all skin interventions were put into place per MD orders. They were also educated on how to find interventions in the care plan/Kardex. Identification of Other Residents: Wound nurse immediately audited (01/14/26) all residents with wounds to ensure all treatments were completed per MD orders and audited to ensure all skin preventative interventions were in place. No further affected residents identified. Systems and Measures: Education for all nurses was immediately initiated on 1/14/26. Education included following wound treatments as ordered per MD and who to contact if assistance is required to fulfill MD order. In addition, the education included ensuring all interventions are in place and how to locate those interventions (care plan/Kardex). Monitoring: The Director of Nursing or designee will complete audits to ensure all wound treatments are followed per MD and monitoring to ensure all interventions are in place as ordered and per resident care plan. This audit will take place 3 times weekly for 90 days. Audit form will include date, resident name, location of wound(s), if the treatment order was completed per MD, if skin preventative interventions are in place per resident care plan and a section for notes/education provided. Monitoring will be included in monthly QAPI.
0698Dialysis▼
Findings
Based on record review and interviews, the facility failed to ensure residents who required dialysis services received such services consistent with professional standards of practice for one (#10) of one resident reviewed for dialysis out of 37 sample residents. Specifically, the facility failed to consistently complete the communication form used for dialysis communication for Resident #10Findings include:I. Facility policy and procedureThe Dialysis (Renal), Pre and Post-Care policy and procedure, revised April 2025, was received from the regional consultant on 1/15/26 at 9:02 a.m. It read in pertinent part, “Assist resident in maintaining homeostasis pre- and post-renal dialysis; assess and maintain patency of renal dialysis access; assess resident daily for function related to renal dialysis; participate in ongoing communication and collaboration with the dialysis facility regarding dialysis care and services.“Assess resident’s blood pressure (in non-fistula arm) prior to being transported to the dialysis unit. Any staff concerns about resident’s condition that may influence the dialysis treatment should be addressed prior to leaving skilled facility as the resident may need to be assessed in an emergency room.“Dialysis access should be assessed upon return to the facility for patency, any unusual redness, swelling, or bleeding. Any significant change in medical condition should be reported immediately. Report any fever, unusual fatigue or weakness, shortness of breath, unusual pain, sleeplessness, chest pain, somnolence or any deviation from the resident's norm.“The care of the resident receiving dialysis services will reflect ongoing communication, coordination and collaboration between the nursing home and dialysis staff.“Documentation related to pre- and post-dialysis care will be placed in the clinical record and include: resident assessments, interventions, and any provided education. Assessment of renal dialysis access site, to include presence or absence and quality of a bruit and thrill for residents with an arteriovenous fistula. Communication between facility and dialysis staff or medical provider.”II. Resident #10 A. Resident statusResident #10, age less than 65, was admitted on 12/23/25. According to the January 2026 computerized physician orders (CPO), diagnoses included other disorders of electrolyte and fluid balance, end stage renal disease (abnormal kidney function), type two diabetes (abnormal glucose control). The 1/2/26 minimum data set (MDS) assessment revealed Resident #10 had moderate cognitive impairments with a brief interview for mental status (BIMS) score of eight out of 15. The MDS assessment revealed Resident #10 was dependent on staff for transfers, and lower body dressing and needed substantial to maximal assistance with upper body dressing, toileting, and bathing. The MDS assessment revealed Resident #10 had renal insufficiency, renal failure, or end stage renal disease (ESRD). B. Record reviewThe dialysis communication for Resident #10, from 12/23/25 (the date of the resident’s admission to the facility) through 1/14/26, was provided by nursing home administrator (NHA) #3 on 1/14/26 at 2:16 p.m. Review of the communication revealed three dialysis communication forms, dated 1/1/26, 1/6/26 and 1/13/26.-The 1/1/26 dialysis communication form did not document what medications were administered to Resident #10 prior to dialysis treatment. -The 1/6/26 dialysis communication form did not document a pre-dialysis weight for Resident #10. The 1/13/26 dialysis communication form had all information documented completely on the form.-There were no further dialysis communication forms from 12/23/25 through 1/14/26 provided by the facility. On 1/16/26, after the survey exit, the facility provided additional dialysis communication forms for Resident #10 for 12/27/25, 12/30/25, 1/3/26, 1.8/26 and 1/9/26. The additional dialysis communication forms revealed the following:-The 12/27/25 dialysis communication form did not document what medications were administered to Resident #10 and was not signed by the nurse.-The 12/30/25 dialysis communication form did not document a pre-dialysis weight for Resident #10.-The 1/3/26 dialysis communication form did not document what medications were administered to Resident #10 prior to dialysis and was not signed by the nurse.-The 1/8/26 dialysis communication form did not document what medications were administered to Resident #10 prior to dialysis. -The 1/9/26 dialysis communication form did not document a pre-dialysis weight for Resident #10, did not document what medications were administered to the resident prior to dialysis and was not signed by the nurse.-Additionally, none of the dialysis communication forms provided after the survey exit included the information from the dialysis center on them. III. Staff interviewsLicensed practical nurse (LPN) #1 was interviewed on 1/14/26 at 1:08 p.m. LPN #1 said the facility was using a communication sheet for dialysis communication instead of a notebook. She said the facility would send the communication sheet in a folder to dialysis with the resident. She said the facility filled out the top half of the sheet and the dialysis center filled out the bottom portion. LPN #1 said when the resident came back from dialysis, the medical records staff would upload the form into the resident’s electronic medical record (EMR). The dialysis registered nurse (RN) was interviewed on 1/14/26 at 1:55 p.m. The dialysis RN said she had been working with Resident #10 since before she was admitted to the facility. She said communication with the facility was difficult. She said the facility did not get back to the dialysis center timely. She said the communication form was often not filled out completely. She said most of the time the facility would only fill out the resident’s last vital signs and her diet. She said the facility should be completing the pre-dialysis weight, what medications were administered to the resident prior to dialysis, vital signs and if there was any change in condition for the resident. The dialysis RN said there was a transportation issue on 1/8/26. She said once Resident #10 was finished with her dialysis treatment, no one from the facility was there to pick her up. She said the facility refused to pick her up. She said it took calling the non-emergent paramedics and having them convince the facility to pick the resident up. She said Resident #1 was at the dialysis center for an extra hour and a half to two hours on 1/8/26 because of the transportation issue. She said that on 1/9/26 Resident #10’s treatment was delayed two hours due to the facility forgetting to send her sling for transfers. She said the dialysis center had to call numerous times for the facility to pick up the phone. She said best practice for good communication had been having one point of contact, which was usually the transportation person unless it was high critical needs. RN #5 was interviewed on 1/15/26 at 10:21 a.m. RN #5 said the process for sending a resident to dialysis included administering medications to the resident, taking their vital signs and obtaining their pre-dialysis weight. She said the nurse would write down the resident’s weight and vital signs on the dialysis communication sheet. She said that when the resident came back from dialysis, the nurse would take the resident’s vital signs again and check the resident’s dialysis access site. She said for Resident #1, she would check the resident’s bruit and thrill as well). She said she was unsure if the nurses were supposed to obtain a post-dialysis weight when the resident came back from dialysis. Director of nursing (DON) #1 was interviewed on 1/15/26 at 1:07 p.m. DON #1 said staff knew who had dialysis because there was a physician’s order with the resident’s dialysis chair time, the days the resident went to dialysis and which dialysis center the resident went to. She said that when a resident went to dialysis, the facility would send the dialysis communication form with the resident. DON #1 said the communication form had the resident’s vital signs and pre-dialysis weight documented on it and then the dialysis center would fill out their portion of the form and send it back with the resident. She said the resident’s primary nurse for the day was responsible for filling out the dialysis communication form and the dialysis center was responsible for filling out their portion. She said the communication form was then uploaded into the resident’s EMR upon the resident’s return from the dialysis center. She said the dialysis center would talk to the charge nurse when they called or if the charge nurse was not available, the dialysis center would talk to the DON.DON #1 said she did hear about the transportation issue that had happened on 1/8/26 with Resident #10. She said when Resident #10 was living in the community, her family would cancel her rides, so the transportation company had canceled her service. She said the facility had been working on setting up a new transportation company but the facility van driver had been filling in until they got everything worked out. She said for the missing dialysis communication sheets for the days that Resident #10 went to dialysis, she said the dialysis center did not send the communication sheets back. She said when the dialysis center did not send the communication forms back, she would request the treatment details and they would send them over.
Plan of correction · submitted by the facility
Resident Specific: The facility failed to ensure residents who required dialysis services received such services consistent with professional standards of practice for one (#10) of one resident reviewed for dialysis out of 37 sample residents. The facility failed to consistently complete the communication form used for dialysis communication for Resident #10. The facility requested all information from the dialysis center to be completed in full upon resident return. Facility staff education on ensuring facility information is completed in full before resident departs to dialysis center. Identification of Other Residents:No other residents identified as the facility only has one resident on dialysis at this time. Systems and Measures: DON communicated with dialysis team to ensure communication forms are properly filled out upon resident return. In addition, nurses on the floor educated to fill out facility information in full and to call dialysis and request a completed form in the case the resident returns with a blank communication form. Monitoring: The Director of Nursing or designee will complete audits to ensure compliance is met. This audit will take place 3 times weekly for 90 days. Audit form includes date, resident name, if the facility completed the dialysis form in full, if the dialysis center completed their information in full on the dialysis form and a section for notes/education. In addition, there is a section in the audit form that requests and explanation for action taken in the event there is missing information on the dialysis form. Monitoring will be included in monthly QAPI.
0880Infection Prevention & Control▼
Findings
Based on observations and interviews, the facility failed to ensure infection prevention and control programs (IPCP) were maintained and followed to provide a safe, sanitary and comfortable environment and to help prevent the development and transmission of communicable diseases and infections on two of four units. Specifically, the facility failed to: -Ensure staff followed appropriate hand hygiene and gown changes while performing wound care for Resident #61; and,-Ensure staff wore the appropriate personal protective equipment (PPE) when providing incontinence care and transfers for Resident #70, who was on enhanced barrier precautions (EBP) for wounds. Findings include:I. Failed to ensure staff performed appropriate hand hygiene and gown changes while providing wound care for Resident #61A. Facility policy and procedureThe infection Control policy, undated, was received from nursing home administrator (NHA) #1 on 1/12/26 at 10:26 a.m. The policy read in pertinent part,“It is the policy of this facility to prevent the spread of bloodborne pathogens among healthcare workers by direct or indirect contact with high risk body fluids.“Hand hygiene is required following any resident contact, after touching blood, body fluids, secretions, excretions, contaminated items; immediately after removing gloves, and between resident contacts.“Avoid unnecessary touching of surfaces in close proximity to the resident to prevent both contamination of clean hands from environmental surfaces and transmission of pathogens from contaminated hands to surfaces. “Remove gloves promptly after use and discard before touching non-contaminated items or environmental surfaces, and before providing care to another resident. Wash hands immediately after removing gloves.”B. Resident interviewResident #61 was interviewed on 1/14/26 at 7:45 a.m. Resident #61 said she was admitted to the facility last month for wound care and recovery. She said her wound care involved a wound vac and it was done on Mondays, Wednesdays, and Fridays. She said the nursing staff would wear gloves and a mask when providing her with wound care. She said the nursing staff did not always wear gowns when doing her wound care. She said she did not know if the nursing staff were required to wear a gown during wound care. C. ObservationsOn 1/14/26 at 2:00 p.m. there was a sign on Resident #61’s door that indicated she was on EBP. The sign on the resident’s door indicated gloves and a gown must be worn for resident care activities, including dressing, bathing/showering, transferring, linen changes, providing hygiene, changing briefs or assisting with toileting and device care or use, such as central lines, urinary catheters, feeding tubes, tracheostomies and wound care. On 1/14/26 at 2:12 p.m., during completion of wound care for Resident #61, the assistant director of nursing (ADON) touched the resident’s dresser dresser drawer to retrieve barrier pads to use during wound care while wearing gloves. After touching the resident’s dresser drawer with her gloved hands, the ADON proceeded with the resident’s wound care without changing her gloves or performing hand hygiene. The ADON was immediately notified of the observations made of her contaminating her gloves by touching the resident’s furniture. The ADON said she did not realize what she was doing at the moment and proceeded to remove the dirty gloves, perform hand hygiene with hand sanitizer and put on new clean gloves. On 1/14/26 at 2:14 p.m. an unidentified staff member donned gloves and a gown to assist the ADON with wound care for Resident #61. The unidentified staff member failed to change his gown after rubbing his face on his left arm twice during the wound care. The unidentified staff member was notified of the observation. He said he should not have rubbed his face on the clean gown because of the risk of spreading bacteria. The unidentified staff member proceeded to remove his gown and put on a clean new gown to continue assisting with the ADON with Resident #61’s wound care. II. Failed to ensure staff wore the appropriate PPE when providing incontinence care and transfers for Resident #70, who was on EBP for open wounds on his left foot. A. Professional referenceAccording to the Centers for Disease Control and Prevention’s (CDC) Implementation of Personal Protective Equipment (PPE) Use in Nursing Homes to Prevent Spread of Multidrug-resistant Organisms (MDROs), retrieved on 1/18/26 from https://www.cdc.gov/long-term-care-facilities/hcp/prevent-mdro/PPE.html,"Enhanced barrier precautions (EBP) are an infection control intervention designed to reduce transmission of resistant organisms that employ targeted gown and glove use during high contact resident care activities.“Nursing home residents with wounds and indwelling medical devices are at especially high risk of both acquisition of and colonization with MDROs. The use of gown and gloves for high-contact resident care activities is indicated, when contact precautions do not otherwise apply, for nursing home residents with wounds and/or indwelling medical devices regardless of MDRO colonization, as well as for residents with MDRO infection or colonization.“Examples of high-contact resident care activities requiring gown and glove use for enhanced barrier precautions include dressing, bathing/showering, transferring, providing hygiene, changing linens, changing briefs or assisting with toileting, device care or use (central line, urinary catheter, feeding tube, tracheostomy/ventilator) and wound care, any skin opening requiring a dressing.”B. Observations On 1/12/26 at 10:25 a.m. there was a sign on Resident #70’s door that indicated the resident was on EBP. The sign on the resident’s door indicated gloves and a gown must be worn for resident care activities, including dressing, bathing/showering, transferring, linen changes, providing hygiene, changing briefs or assisting with toileting and device care or use, such as central lines, urinary catheters, feeding tubes, tracheostomies and wound care. On 1/14/26 at 6:53 a.m. certified nurse aide (CNA) #7 was assisting Resident #70, with a toilet to chair transfer. CNA #7 had gloves on, but failed to don a gown while providing direct care to Resident #70. III. Staff interviews CNA #5 was interviewed on 1/13/26 at 8:47 a.m. CNA #5 said she picked up shifts often at the facility through a staffing agency. She said she did not receive any specific training from the facility regarding resident care or facility policy. She said it was typical not to receive any training from the facility as an agency CNA. She said she understood infection control precautions from previous training at other facilities. She said her understanding of EBP was that staff were to wear gowns and gloves when a resident had an indwelling foley catheter, open wounds, indwelling devices or other high contact care such as transferring, dressing and linen changes. CNA #7 was interviewed on 1/14/26 at 7:00 a.m. CNA #7 said she did not wear a gown while providing care for Resident #70 because she did not know he was on precautions. She said she did not recall receiving any specific education regarding EBP from the facility. She said she knew Resident #70 had wounds on his feet, but thought she was only required to wear gloves while providing care. Licensed practical nurse (LPN) #2 was interviewed on 1/14/26 at 8:30 a.m. LPN #2 said any resident with an indwelling foley catheter or open wound required gowns and gloves for nursing staff to perform care. The infection preventionist (IP) and director of nursing (DON) #1 were interviewed together on 1/15/26 at 10:10 a.m. The IP said she was responsible for monitoring and tracking infection trends in the facility. The IP said it was very important to adhere to infection control standards while providing care to residents to minimize the spread of bacteria. The IP said all nursing staff in the facility were provided education regarding EBP during newemployee orientation. The IP said she also provided infection control education quarterly to all nursing staff. The IP said she would start to conduct more audits and education for the nursing staff regarding preventing the spread of bacteria through transmission based precautions. DON #1 said the ADON was very nervous while being observed performing wound care for Resident #61. DON #1 said she would immediately provide education to both the ADON and the unidentified staff member, along with the rest of the direct care nursing staff regarding infection control protocol with hand hygiene and gown changes. DON #1 said Resident #61 was at a high risk of getting an infection because she had a very complicated wound. DON #1 said the importance of maintaining strict transmission based precautions was critical to prevent Resident #61 and Resident #70 from acquiring an infection.
Plan of correction · submitted by the facility
Resident Specific: The facility failed to ensure infection prevention and control programs (IPCP) were maintained and followed to provide a safe, sanitary and comfortable environment and to help prevent the development and transmission of communicable diseases and infections on two of four units. The facility failed to ensure staff followed appropriate hand hygiene and gown changes while performing wound care for Resident #61and failed to ensure staff wore the appropriate personal protective equipment (PPE) when providing incontinence care and transfers for Resident #70, who was on enhanced barrier precautions (EBP) for wounds. Staff re-educated on infection control practices on 01/15/26 when notified of the facility failure. Identification of Other Residents: An audit was completed by IPC.- It was noted some staff were not wearing appropriate PPE when entering rooms and providing cares that required PPE precautions. Systems and Measures: SDC (staff development coordinator)/designee initiated an education for all staff on infection control practices on the day facility noted errors were made (01/15/26). The education included when to wear PPE and examples of residents that require it. The education also included following infection control practices during wound care for those residents who require enhanced barrier precautions. Monitoring: The Director of Nursing or designee will complete audits to ensure infection prevention & control practices are followed per facility protocol. This audit will take place 3 times weekly for 90 days. Two different audit forms will be monitored. Audit #1 includes resident name, hall, if appropriate PPE was worn, if hand hygiene was acceptable per facility protocol, if incontinence care was provided and if infection control practices were followed. Audit #2 includes, resident name, hall, if appropriate PPE was worn, if hand hygiene was acceptable per facility protocol and if gown changes were acceptable per facility protocol. Monitoring will be included in monthly QAPI.
0881Antibiotic Stewardship Program▼
Findings
Based on observations, record review and interviews, the facility failed to develop an antibiotic stewardship program that promotes the appropriate use of antibiotics and includes a system of monitoring to improve resident outcomes and reduce antibiotic resistance for one (#8) of five residents out of 37 sample residents. Specifically, the facility failed to ensure clinical signs and symptoms of side effects and adverse reactions were monitored and identified for Resident #8 while the resident was receiving prescribed antibiotics. Findings include:I. Professional referenceThe Centers for Disease Control and Prevention’s (CDC) Antibiotic Prescribing and Usage in Hospitals and Long-term Care, dated 2019, was retrieved on 1/16/26 from https://www.cdc.gov/antibiotic-use/hcp/core-elements/hospital.html. It read in pertinent part,"Implement policies that apply in all situations to support antibiotic prescribing to include specifying the dose, duration and indication for all courses of antibiotics so that they are readily identifiable. Implement facility specific treatment recommendations, based upon the national guidelines and local susceptibilities and formulary options that optimizes antibiotic selections, duration, and common indications for the usage of community acquired pneumonia, urinary tract infections, skin and soft tissue infections."II. Facility policy and procedureThe Antibiotic Stewardship policy, dated September 2017, was received from nursing home administrator (NHA) #1 on 1/12/26 at 10:26 a.m. The policy read in pertinent part, “It is the policy of this facility to implement an Antibiotic Stewardship Program (ASP) that is incorporated in the overall Infection Prevention and Control Program which will promote appropriate use of antibiotics while optimizing the treatment of infections, at the same time reducing the possible adverse events associated with antibiotic use. This policy has the potential to limit antibiotic resistance in the post-acute care setting, while improving treatment efficacy and resident safety, and reducing treatment-related costs.“The team will review data, monitor and summarize antibiotic use from pharmacy data, such as the rate of new starts, types of antibiotics prescribed, or days of antibiotic treatment per 1,000 resident days. Summarize antibiotic resistance patterns based on laboratory data. Incorporate monitoring of antibiotic use, including the frequency of monitoring/review. Report on the number of antibiotics prescribed and the number of residents treated each month and assess residents for any infection using McGeer’s criteria.”III. Resident #8 A. Resident statusResident #8, age less than 65, was admitted on 4/26/24 and readmitted on 1/7/26. According to the January 2026 computerized physician orders (CPO), diagnoses included obstructive uropathy (a condition where urine flow is blocked, causing a backup of urine into the kidneys), dementia, transient ischemic attack (TIA), epilepsy and spinal stenosis. According to the 11/24/25 minimum data set (MDS) assessment, Resident #8 had moderate cognitive impairment with a brief interview for mental status (BIMS) score of 11 out of 15. He was dependent on staff assistance and required two or more staff members for toileting hygiene, dressing and bathing. The MDS assessment revealed the resident was receiving an antibiotic medication and had an indwelling urinary catheter. B. Resident interview Resident #8 was interviewed on 1/13/26 at 1:30 p.m. Resident #8 said he did not eat by mouth because he had the gastrostomy feeding tube (G-tube) R said he had a catheter because he retained urine. Resident #8 did not think he had any infections but was aware he was taking an antibiotic medication. He said he did not know what side effects of the medication to watch for. C. Record review Review of Resident #8’s January 2026 CPO revealed the following physician's order:Cefuroxime Axetil (antibiotic) oral tablet 500 milligrams (mg). Give one tablet by G-tube two times a day for urinary tract infection (UTI) for three days, ordered 1/13/26. Review of Resident #8’s electronic medical record (EMR) revealed alert charting to monitor the resident’s urinary tract infection. The monitoring included abnormal urine color, cloudy urine, hematuria (blood in the urine) and bladder spasms.-There was no documentation in the resident's EMR to indicate antibiotic side effects were consistently being reviewed and monitored. Resident #8’s infection care plan revealed he had a risk for infection related to indwelling devices, including a suprapubic catheter and an internal feeding device (initiated 9/10/24). Interventions included enhanced barrier precautions, monitoring for signs and symptoms of infection, monitoring vital signs and educating the resident, family and caregivers regarding the importance of hand washing. -However, the resident’s care plan revealed no specific interventions for caregivers to monitor for side effects related to the use of antibiotics. IV. Staff interviews Certified nurse aid (CNA) #8 was interviewed on 1/11/26 at 2:02 p.m. She said she worked at the facility through a staffing agency. She said the long-term hall residents required mechanical lifts, incontinence care, and fall risk monitoring. She said she did not do any monitoring for antibiotics for Resident #8 because that was not her role. She said if she noticed any behavior that was unusual for any residents, she would report it to the floor nurses. She said some days the nursing staff would work with not enough help. She said if she worked shorthanded, it would affect her ability to provide care and notice changes in the residents. \Licensed practical nurse (LPN) #2 was interviewed on 1/14/26 at 8:30 a.m. LPN #2 said the nurses were responsible for performing catheter care for the residents every shift. She said Resident #8 was on an antibiotic for a urinary tract infection. She said the nursing staff would monitor the resident to make sure the antibiotic was effective. She said the nursing staff would also monitor for side effects of taking the antibiotics. She said side effects of taking antibiotics included nausea, vomiting or upset stomach. She said the nurses would document the side effects of the antibiotic in the nursing progress notes.-However, there was no documentation in Resident #8’s EMR to indicate side effects of the antibiotic medication were being monitored for the resident (see record review above). The infection preventionist (IP) and director of nursing (DON) #1 were interviewed together on 1/15/26 at 10:10 a.m. The IP said She is responsible for monitoring and tracking infection trends in the facility. The IP said every resident who has an indwelling urinary catheter would also have a care plan for catheter care to prevent urinary tract infection. The IP said if a resident was on antibiotics for an infection, the nurses would monitor for the effectiveness of the antibiotic, in addition to adverse reactions to the antibiotic. She said this monitoring would be documented in the residents’ EMR. She said all residents who were taking antibiotics should have a care plan with interventions for the nursing staff to utilize. DON #1 said Resident #8 received an order from the physician for an additional three days of antibiotic therapy for his urinary tract infection. She said the nurses were aware of the need to monitor for and document adverse reactions while residents were receiving antibiotics. She said there was no monitoring documentation placed in Resident #8’s EMR. She said she assumed that the nurses would document this information in the progress notes. She said she would make sure all residents who were on antibiotics had specific antibiotic adverse reaction monitoring documentation. DON #1 said it was always important to monitor when residents were taking short-term antibiotics to prevent unwanted side effects.
Plan of correction · submitted by the facility
Resident Specific: The facility failed to develop an antibiotic stewardship program that promotes the appropriate use of antibiotics and includes a system of monitoring to improve resident outcomes and reduce antibiotic resistance for one (#8) of five residents out of 37 sample residents. The facility failed to ensure clinical signs and symptoms of side effects and adverse reactions were monitored and identified for Resident #8 while the resident was receiving prescribed antibiotics. IP and nurses were educated on the day error was noted (01/15/26). Identification of Other Residents:IP/DON completed an audit of all residents who were on antibiotics. IP had a log of all antibiotics that were being tracked and infection surveillance UDA’s completed. IP also followed McGreer’s criteria. It was noted that nurses on the floor needed education on follow up documentation regarding antibiotic monitoring and that facility care plans needed updating to reflect antibiotic use and sign/symptoms of side effects. Systems and Measures:Nursing staff educated on the need for follow up documentation regarding antibiotics. This included monitoring for side effects and adverse reactions. IP educated on ensuring antibiotic use and sign and symptoms of antibiotic use be included in the resident plan of care. Monitoring: The Director of Nursing or designee will complete audits to ensure antibiotic stewardship is followed per facility protocol .This audit will take place 3 times weekly for 90 days. Audit form includes date, resident name, antibiotic ordered, if it meets McGreer’s criteria, if infection surveillance UDA was completed, if alert charting was initiated to include signs and symptoms of side effects (for 72 hours) and if the care plan was updated to reflect antibiotic use and has signs and symptoms of side effects documented. Monitoring will be included in monthly QAPI.
Reportable Occurrences
65 records6/18/2026Physical Abuse · ID 26020332014Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 6/18/26, the healthcare entity investigated a reportable event. The facility acted appropriately to protect their clients by taking immediate protective actions, investigating the event, and implementing a plan to help prevent a future recurrence. The healthcare entity reported physical abuse of a client. Staff entered the room and found two clients holding onto each other’s arms. During the course of the investigation, the healthcare entity separated the clients prior to notifying law enforcement, assessed the clients, and conducted interviews. Client (A) sustained a bruise to their wrist requiring no treatment. Both clients indicated they grabbed each other to try to show the other client where the exit door was located. Both clients denied any aggression or intent to harm, and denied pain. The facility determined physical contact occurred as a result of both clients trying to provide directions to each other. The facility initiated increased safety monitoring and provided additional staff on the unit to ensure increased monitoring. The event was not substantiated. This public occurrence summary was provided in accordance with 25-1-124, C.R.S., and was based on the report and investigation provided by the licensed healthcare entity. Department investigation of this occurrence was conducted off-site. The healthcare entity occurrence report was submitted within the required timeframe.
Publication
Sent to facility 7/24/2026 · released to the public 7/31/2026.
6/4/2026Physical Abuse · ID 26020332010Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 6/4/26, the healthcare entity investigated a reportable event. The facility acted appropriately to protect their clients by taking immediate protective actions, investigating the event, and implementing a plan to help prevent a future recurrence. The healthcare entity reported physical abuse of a client. Reportedly, client (B) made physical contact with client (A) while conversing in the common area. During the course of the investigation, the healthcare entity separated the clients prior not notifying law enforcement, assessed the client, and conducted interviews. Neither client had any visible injuries. Both clients denied any physical contact occurred. Two staff members witnessed the event, one reported physical contact occurred and one reported no physical contact occurred. The facility was unable to confirm physical abuse occurred due to inconclusive evidence. The facility completed a referral for behavioral health, added staff to the unit, initiated increased safety monitoring, completed a medication review, and educated staff regarding new interventions. The event was not substantiated. This public occurrence summary was provided in accordance with 25-1-124, C.R.S., and was based on the report and investigation provided by the licensed healthcare entity. Department investigation of this occurrence was conducted off-site. The healthcare entity occurrence report was submitted within the required timeframe.
Publication
Sent to facility 7/28/2026 · released to the public 8/4/2026.
5/10/2026Physical Abuse · ID 26020332008Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 5/10/26, the healthcare entity investigated a reportable event. The facility acted appropriately to protect their clients by taking immediate protective actions, investigating the event, and implementing a plan to help prevent a future recurrence. The healthcare entity reported physical abuse of a client. Staff witnessed client (B) pinch client (A) on the arm. During the course of the investigation, the healthcare entity separated the clients prior to notifying law enforcement, assessed the client, initiated increased safety monitoring, and conducted interviews. Client (A) sustained a discolored mark on their arm requiring no treatment. Client (B) could not recall the event due to cognitive impairment. The facility initiated line of sight monitoring for a period of time, completed a medication review, and adjusted seating arrangements to avoid unsupervised contact between the clients. The event was substantiated. This public occurrence summary was provided in accordance with 25-1-124, C.R.S., and was based on the report and investigation provided by the licensed healthcare entity. Department investigation of this occurrence was conducted off-site. The healthcare entity occurrence report was submitted within the required timeframe.
Publication
Sent to facility 7/13/2026 · released to the public 7/20/2026.
4/29/2026Physical Abuse · ID 26020332007Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 4/29/26, the healthcare entity investigated a reportable event of physical abuse of a client. Staff #2 reported staff #1 was verbally aggressive with the client and made contact with the client’s shoulder. During the course of the investigation, the healthcare entity notified law enforcement, suspended staff, conducted interviews, and assessed the client. The client did not have any visible injuries. The client was unable to recall the event due to cognitive impairment. Staff #1 denied the allegations, indicated they verbally redirected the client, and guided the client away from the area. The facility was unable to determine if physical abuse occurred due to inconclusive evidence. Staff #1 did not return to work at the facility. The event was not substantiated. This public occurrence summary was provided in accordance with 25-1-124, C.R.S., and was based on the report and investigation provided by the licensed healthcare entity. The department review of the occurrence investigation was conducted off-site. The healthcare entity occurrence report was submitted within the required timeframe. In addition, this event has been identified for further investigation by the Department. An onsite investigation was conducted by a representative from the State agency. For results of that on-site investigation, please reference https://cdphe.colorado.gov/find-and-compare-facilities, specifically the inspection dated 5/19/26, Event ID 232887-H1.
Publication
Sent to facility 6/26/2026 · released to the public 7/3/2026.
3/26/2026Physical Abuse · ID 26020332005Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 3/26/26, the healthcare entity investigated a reportable event. The facility acted appropriately to protect their clients by taking immediate protective actions, investigating the event, and implementing a plan to help prevent a future recurrence. The healthcare entity reported physical abuse of a client. Staff entered the room while the client was visiting with a family member and noted a red mark resembling a handprint on the client’s chest. During the course of the investigation, the healthcare entity notified law enforcement, conducted interviews, assessed the client, escorted the family member off the property, and started increased safety monitoring. The client’s family member denied hitting the client and reported they believed the client had been hit by their roommate. The client reported their family was responsible for the mark on their chest. The client indicated they did not want the family member to come to the facility for visits any longer. The facility suspended the family member’s visitation privileges, offered therapeutic support, and continued increased monitoring. The facility was unable to confirm physical abuse due to inconclusive evidence as no person witnessed the event and there were conflicting interviews from the client and family member. Law enforcement and Adult Protection Services conducted separate investigations. The event was not substantiated. This public occurrence summary was provided in accordance with 25-1-124, C.R.S., and was based on the report and investigation provided by the licensed healthcare entity. Department investigation of this occurrence was conducted off-site. The healthcare entity occurrence report was submitted within the required timeframe.
Publication
Sent to facility 6/17/2026 · released to the public 6/24/2026.
3/1/2026Sexual Abuse · ID 26020332006Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 3/31/26, the healthcare entity investigated a reportable event. The facility acted appropriately to protect their clients by taking immediate protective actions, investigating the event, and implementing a plan to help prevent a future recurrence. The healthcare entity reported a sexual abuse event. A representative from Adult Protective Services showed up to investigate an alleged sexual assault incident involving client (A). During the course of the investigation, the healthcare entity started frequent safety checks, offered emergency services and notified the police. Management also conducted interviews and record reviews. Client (A) reported the alleged assault occurred at a different facility a while ago and no further details could be recalled. Client (A)'s family member reported an allegation of a sexual incident that occurred in this facility about a month ago but did not report it until now. Client (A) reported the sexual incident did not happen as the family alleged. No other clients reported having any concerns about a violation of their personal boundaries. Client (A)'s care plan was updated to reflect female caregivers only for personal care. The event was not substantiated. This public occurrence summary was provided in accordance with 25-1-124, C.R.S., and was based on the report and investigation provided by the licensed healthcare entity. Department investigation of this occurrence was conducted off-site. The healthcare entity occurrence report was submitted within the required timeframe.
Publication
Sent to facility 6/10/2026 · released to the public 6/17/2026.
2/18/2026Physical Abuse · ID 26020332004Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 2/19/26, the healthcare entity investigated a reportable event. The facility acted appropriately to protect their clients by taking immediate protective actions, investigating the event, and implementing a plan to help prevent a future recurrence. The healthcare entity reported physical abuse of a client The client initially reported staff repositioned in a way that caused pain to their leg, head, and threw glasses at them. During the course of the investigation, the healthcare entity notified law enforcement, suspended staff, assessed the client, and conducted interviews. Upon further interview the client indicated they didn’t think staff intended any harm and accidentally hurt their leg and recanted the allegation regarding the glasses. Staff #1 denied the allegations of cousin pain and other staff members reported the client reported pain and said they believed the pain was caused by accident. The facility determined staff caused pain by accident when repositioning the client. The facility implemented a two person care model, and educated staff regarding repositioning techniques. The event was not substantiated. This public occurrence summary was provided in accordance with 25-1-124, C.R.S., and was based on the report and investigation provided by the licensed healthcare entity. Department investigation of this occurrence was conducted off-site. The healthcare entity occurrence report was submitted within the required timeframe.
Publication
Sent to facility 5/21/2026 · released to the public 5/28/2026.
2/4/2026Physical Abuse · ID 26020332003Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 2/4/26, the healthcare entity investigated a reportable event. The facility acted appropriately to protect their clients by taking immediate protective actions, investigating the event, and implementing a plan to help prevent a future recurrence. The healthcare entity reported physical abuse of a client. Staff witnessed client (B) hit client (A) in the cheek and when client (A) tried to block the hit, they made contact with client (B)’s head. During the course of the investigation, the healthcare entity separated the clients prior to notifying law enforcement, assessed the clients, started increased safety monitoring, and conducted interviews. Neither client sustained visible injuries. Staff interviews indicated the event started when the clients accidentally bumped into each other’s wheelchairs. The facility offered room changes, educated staff, and offered alternative dining room seating arrangements. The event was substantiated. This public occurrence summary was provided in accordance with 25-1-124, C.R.S., and was based on the report and investigation provided by the licensed healthcare entity. Department investigation of this occurrence was conducted off-site. The healthcare entity occurrence report was submitted within the required timeframe.
Publication
Sent to facility 5/19/2026 · released to the public 5/26/2026.
1/14/2026Physical Abuse · ID 26020332002Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 1/11/26, the healthcare entity investigated a reportable event. The facility acted appropriately to protect their clients by taking immediate protective actions, investigating the event, and implementing a plan to help prevent a future recurrence. The healthcare entity reported physical abuse of a client. A bruise was found on the client’s eye. During the course of the investigation, the healthcare entity notified law enforcement, conducted interviews, and assessed the client. The client’s spouse took them to the hospital for evaluation and there were no findings other than the bruise. The client did not know how the bruise occurred and denied any physical contact with staff or other clients. Staff interviews revealed the client often laid their head on the table and frequently bent over to pick up items that may or may not be present, and had occasionally hit their head when standing back up. The facility padded all furniture in the client's room that had sharp edges. The event was not substantiated. This public occurrence summary was provided in accordance with 25-1-124, C.R.S., and was based on the report and investigation provided by the licensed healthcare entity. Department investigation of this occurrence was conducted off-site. The healthcare entity occurrence report was submitted within the required timeframe.
Publication
Sent to facility 5/11/2026 · released to the public 5/18/2026.
12/27/2025Physical Abuse · ID 25020332022Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 12/27/25, the healthcare entity investigated a reportable event. The facility acted appropriately to protect their clients by taking immediate protective actions, investigating the event, and implementing a plan to help prevent a future recurrence. The healthcare entity reported physical abuse of a client. The client alleged staff restrained them when they attempted to get out of their chair. During the course of the investigation, the healthcare entity suspended staff, reviewed records, notified law enforcement, assessed the client, and conducted interviews. An assessment showed discoloration on the clients arm. Upon interview the client could not recall the event. Staff denied the allegations and reported getting the client up and bringing them to the common area. Record review showed the client had recent medication adjustment, was recovering from a urinary tract infection, and had been hitting the walls with their arms. The facility determined the discoloration on the client’s arm was the result of striking the walls. The facility updated the care plan with new interventions and medication adjustments, and educated staff. The event was not substantiated. This public occurrence summary was provided in accordance with 25-1-124, C.R.S., and was based on the report and investigation provided by the licensed healthcare entity. Department investigation of this occurrence was conducted off-site. The healthcare entity occurrence report was submitted within the required timeframe.
Publication
Sent to facility 4/3/2026 · released to the public 4/13/2026.