21
Inspections
33
Deficiencies
0
Actual Harm or Above
18
Occurrences
July 8, 2026
Last Inspection
S/S D/E/F Potential for harm
The most recent inspection of CONTINUING CARE AT WIND CREST on record is dated July 8, 2026. Across 21 published inspections, state surveyors cited 33 deficiencies, none of which reached the actual-harm level.
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 (Medicare Only)
Administrator
Ficca, Kelsey J
Owner
WIND CREST, INC
Phone
(303) 876-8349
Payor Source
Medicare, Private Pay
City
HIGHLANDS RANCH
ZIP
80129
Inspections & Citations
21 inspections · 33 deficiencies7/8/2026Recertification Survey · ID 235202-L17 deficiencies▼
0000INITIAL COMMENTSSurveyor note▼
Findings
INITIAL COMMENTS (ID Prefix Tag #K000) are informational only and represent the facility's general characteristics. This survey was conducted in accordance with the Federal Register at Section 42 CFR 483.70(a). The facility occupies the first floor of a three-story, Type II (222) construction. The facility is protected by a National Fire Protection Association (NFPA) 13 automatic fire suppression system and is classified as Fully Sprinkled. Floors two (2) and Three (3) are occupied by an Assistant Living (Large Board and Care) occupancy. The facility was constructed in 2013 and is licensed for 44 beds. This re-certification survey, conducted on July 8, 2026, was conducted to comply with the National Fire Protection Association (NFPA 101) Life Safety Code (2012) "Chapter 19, Existing Health Care Occupancies". The deficiencies cited were discussed with the Administrator and Maintenance Director during the exit conference conducted at the exit conference.
Plan of correction
The state did not require a plan of correction for this citation.
0293Exit Signage▼
Findings
Based on observation and staff interviews, it was determined that the facility failed to arrange and maintain exit signage in accordance with Life Safety Code Section 7.10.1.2.1 and Chapter 19. The deficient practice affected all smoke compartments. The deficient practice could affect all smoke zones,44 of 44 residents, and an indeterminable number of staff and visitors. During the record review, observations and interviews with the maintenance director revealed that the annual 90-minute test was not performed. NFPA 101 7.9.3.1 Required emergency lighting systems shall be tested in accordance with one of the three options offered by 7.9.3.1.1, 7.9.3.1.2, or 7.9.3.1.3.7.9.3.1.1 Testing of required emergency lighting systems shall be permitted to be conducted as follows:(1) Functional testing shall be conducted monthly, with a minimum of 3 weeks and a maximum of 5 weeks between tests, for not less than 30 seconds, except as otherwise permitted by 7.9.3.1.1(2).(2)*The test interval shall be permitted to be extended beyond 30 days with the approval of the authority having jurisdiction.(3)Functional testing shall be conducted annually for a minimum of 1 1/2 hours if the emergency lighting system is battery powered.(4)The emergency lighting equipment shall be fully operational for the duration of the tests required by 7.9.3.1.1(1) and (3).(5)Written records of visual inspections and tests shall be kept by the owner for inspection by the authority having jurisdiction. The maintenance director discussed deficient items at the exit conference.
Plan of correction · submitted by the facility
Corrective Action takenThe 90-minute annual inspection was completed on 7/22/2026. Systemic Changes The audit form was modified to clearly delineate emergency exit signs from the remainder of all emergency lighting testing. Monitoring PlanThe monitoring procedure to ensure the PoC is effective and the specific deficiency cited remains corrected and/or in compliance with the regulatory requirements is, the Senior Facility Manager and/or designee will review completion of exit signage inspections to ensure it was completed timely and accurately and to ensure timely follow-up is corrected if identified. Maintenance Supervisor and/or designee will report results to QAPI annually.
0321Hazardous Areas - Enclosure▼
Findings
Based on observation and staff interviews during the survey, it was determined that the facility failed to maintain hazard areas in accordance with NFPA 101, 99, 80, and 58. The deficient practice affected all smoke compartments. The deficient practice could affect all smoke zones,44 of 44 residents, and an indeterminable number of staff and visitors. 1. During the inspection, observations and interviews with the maintenance director revealed that fire door labels by the elevator were painted throughout. 2. During the inspection, observations and interviews with the maintenance director revealed that there was no patching in the therapy mechanical room. 8.7.1.1* Protection from any area having a degree of hazard greater than that normal to the general occupancy of the building or structure shall be provided by one of the following means:Enclosing the area with a fire barrier without windows that has a 1-hour fire resistance rating in accordance with Section 8.3Protecting the area with automatic extinguishing systems in accordance with Section 9.7Applying both 8.7.1.1(1) and (2) where the hazard is severe or where otherwise specified by Chapters 11 through 43NFPA 101 8.3.3.1 Openings required to have a fire protection rating by Table 8.3.4.2 shall be protected by approved, listed, labeled fire door assemblies and fire window assemblies and their accompanying hardware, including all frames, closing devices, anchorage, and sills in accordance with the requirements of NFPA 80, Standard for Fire Doors and Other Opening Protectives, except as otherwise specified in this CodeNFPA 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 805.2.5.1 Fire door assemblies shall be visually inspected from both sides to assess the overall condition of door assembly. 5.2.5.2 The following items shall be verified:(1)No open holes or breaks exist in surfaces of either the door or frame.(2)Slats, endlocks, bottom bar, guide assembly, curtain entry hood, and flame baffle are correctly installed and intact.(3)Glazing, vision light frames, and glazing beads are intact and securely fastened in place, if so equipped.(4)Curtain, barrel, and guides are aligned, level, plumb, and true.(5)Expansion clearance is maintained in accordance with manufacturer’s listing.(6)Drop release arms and weights are not blocked or wedged.(7)Mounting and assembly bolts are intact and secured.(8)Attachments to jambs are with bolts, expansion anchors, or as otherwise required by the listing.(9)Smoke detectors, if equipped, are installed and operational.(10)No parts are missing or broken.(11)Fusible links, if equipped, are in the location; chain/cable, s-hooks, eyes, and so forth, are in good condition (i.e., no kinked or pinched cable, no twisted or inflexible chain); and links are not painted or coated with dust or grease.(12)Auxiliary hardware items that interfere or prohibit operation are not installed on the door or frame.(13)No field modifications to the door assembly have been performed that void the label. The maintenance director discussed deficient items at the exit conference.
Plan of correction · submitted by the facility
Corrective Action takenThe scab patching was corrected on 7/14/2026, to ensure the drywall repairs are flush with the ceiling. Systemic Changes The CC Maintenance Supervisor and/or designee will educate maintenance team to inform them of proper drywall repair technique by 7/23/2026. Monitoring PlanContinuing Care Maintenance Supervisor and/or designee will audit all future drywall repairs to ensure proper technique and consideration of fire rated compartments are prioritized. Results of all future drywall repairs will be reported to QAPI monthly for 90 days.
0324Cooking Facilities▼
Findings
Based on observation it was determined that the facility failed to maintain the kitchen hood suppression system as required by NFPA 96, (Chapter 12, Section 12.1.2.3.1) and cooking appliance restraint as required by NFPA 54, 9.6.1.2. The deficient practice affected 1 of 4 smoke compartments. The deficient practice could affect all smoke zones,13 of 44 residents, and an indeterminable number of staff and visitors. 1. During the inspection, observations and interviews with the maintenance director revealed that commercial cooking equipment under the suppression system does not have wheel blocks installed
2. During the inspection, observations and interviews with the maintenance director revealed that commercial cooking equipment on casters does not have restraint devices installed NFPA 96, 12.1.2.3 The fire-extinguishing system shall not require reevaluation where the cooking appliances are moved for the purposes of maintenance and cleaning, provided the appliances are returned to approved design location prior to cooking operations. NFPA 54 -2012 Fuel and Gas Code 9.6.1.2 Restraints. Movement of appliances with casters shall be limited by a restraining device installed in accordance with the connector and appliance manufacturer installation instructions. The maintenance director discussed deficient items at the exit conference.
Plan of correction · submitted by the facility
Corrective Action takenThe community installed chocks and tethers for all required kitchen equipment on 7/20/2026. Systemic Changes The Dining General Manager and/or designee will educate culinary teams to ensure proper chocking and tethering post cleaning. Monitoring PlanContinuing Care Dining General Manager and/or designee will audit all kitchen equipment weekly, followed by monthly for 60 days. Results will be documented in audit tool. Audit tools will be reported to QAPI monthly for 90 days for further interventions or monitoring as indicated.
0353Sprinkler System - Maintenance and Testing▼
Findings
Based on a record review, observations, inspection, and interviews, it was determined that the facility failed to meet the protection requirements in accordance with NFPA 101, 25, and 13. The deficient practice affected 1 of 4 smoke compartments. The deficient practice could affect all smoke zones,13 of 44 residents, and an indeterminable number of staff and visitors. During the inspection, observations and interviews with the maintenance director revealed that the dry barrel sprinkler heads for the fridge/freezer area were over 5 years old. 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. A.5.3.1.1.2 Examples of these environments are paper mills, packing houses, tanneries, alkali plants, organic fertilizer plants, foundries, forge shops, fumigation areas, pickle and vinegar works, stables, storage battery rooms, electroplating rooms, galvanizing rooms, steam rooms of all descriptions including moist vapor dry kilns, salt storage rooms, locomotive sheds or houses, driveways, areas exposed to outside weather, around bleaching equipment in flour mills, all portions of cold storage areas, and portions of any area where corrosive vapors prevail. Harsh water environments include water supplies that are chemically reactive. The maintenance director discussed deficient items at the exit conference.
Plan of correction · submitted by the facility
Corrective Action takenSprinkler heads exceeding 5 years old in walk-in coolers and freezer have been measured and ordered. Both sprinkler heads are scheduled to be replaced upon delivery, no later than 8/14/2026. Systemic Changes All sprinkler heads in walk-in coolers and freezer have been audited for compliance and expiration. The Security and Emergency Services Manager and/or designee will educate future Sprinkler System vendors/contractors, informing them of NFPA Standards for inspection, testing, and maintenance of water-based fire protection systems. Monitoring PlanThe Security and Emergency Services Manager and/or designee will audit future vendor/contractor services pertaining to the kitchen walk-in and/or freezer to ensure proper NFPA standards are accounted for. Results of future sprinkler system inspections, tests, and maintenance will be reported to QAPI monthly for 90 days.
0355Portable Fire Extinguishers▼
Findings
K355 | Extinguisher Height | Class KBased on observations and a review of records, it was determined that the facility did not maintain fire extinguishers in accordance with NFPA 10. The deficient practice affected 1 of 4 smoke compartments. The deficient practice could affect all smoke zones,13 of 44 residents, and an indeterminable number of staff and visitors. During the inspection, observations and interviews with the maintenance director revealed that the K class fire extinguisher sign was missing. 5.5.5.3* A placard shall be conspicuously placed near the extinguisher that states that the fire protection system shall be actuated prior to using the fire extinguisher. The maintenance director discussed deficient items at the exit conference.
Plan of correction · submitted by the facility
Corrective Action takenAll K class fire extinguishers have signage. Systemic Changes All K class fire extinguishers have been audited for signage. The Security and Emergency Services Manager and/or designee will educate team on components of fire extinguisher monthly audits to include proper signage. Monitoring PlanThe Security and Emergency Manager and/or designee will audit all K class fire extinguishers weekly for 30 days, followed by monthly for 60 days. Results will be documented in audit tool. Results of audits will be reported to QAPI monthly for 90 days.
0914Electrical Systems - Maintenance and Testing▼
Findings
Based on the documentation review, it was determined that the facility did not maintain proper electrical practices in accordance with NFPA 99 Health Care Facilities Code (2012). The deficient practice affected all smoke compartments. The deficient practice affected all smoke compartments. The deficient practice could affect all smoke zones,44 of 44 residents, and an indeterminable number of staff and visitors. During the record review, observations and interviews with the maintenance director revealed that there was no written documentation of the continuity of the grounding circuit, the polarity of the hot and neutral connections, and the retention force of the grounding blade in patient care. These assessments were not conducted annually. NFPA Standard: NFPA 99 Health Care Facilities Code (2012)6.3.3.2 Receptacle Testing in Patient Care Rooms. 6.3.3.2.1 The physical integrity of each receptacle shall be confirmed by visual inspection. 6.3.3.2.2 The continuity of the grounding circuit in each electrical receptacle shall be verified. 6.3.3.2.3 Correct polarity of the hot and neutral connections in each electrical receptacle shall be confirmed. 6.3.3.2.4 The retention force of the grounding blade of each electrical receptacle (except locking-type receptacles) shall be not less than 115 g (4 oz). The administrator and maintenance director discussed deficient items at the exit conference.
Plan of correction · submitted by the facility
Corrective Action takenThe annual load bank inspection was completed by vendor Cummins, on 7/21/2026. Systemic Changes The Continuing Care Director has educated the Senior Facility Manager and CC Maintenance Supervisor of the NFPA requirement: the generator must undergo an annual load bank test lasting for at least 90 minutes, within 12 months of the last load bank test. Monitoring PlanThe monitoring procedure to ensure the PoC is effective and the specific deficiency cited remains corrected and/or in compliance with the regulatory requirements is, the Senior Facility Manager or designee will review completed generator inspections to ensure timely completion and timely follow-up should items be identified. Maintenance Supervisor and/or designee will report annual load bank testing results to QAPI annually.
0918Electrical Systems - Essential Electric Syste▼
Findings
Based on observation and record review during the survey, it was determined that the facility failed to maintain emergency power systems in accordance with Section 9.1.3 ofthe Life Safety Code and the referenced NFPA 110, Standard for Emergency and Standby Power Systems Chapter 8. The deficient practice affected all smoke compartments. The deficient practice affected all smoke compartments. The deficient practice could affect all smoke zones,44 of 44 residents, and an indeterminable number of staff and visitors. During the record review, observations and interviews with the maintenance director revealed that the Missing annual load test8.4.2.4* Diesel-powered EPS installations that do not meet the requirements of 8.4.2 shall be exercised monthly with the available EPSS load and shall be exercised annually with supplemental loads at not less than 50 percent of the EPS nameplate kW rating for 30 continuous minutes and at not less than 75 percent of the EPS nameplate kW rating for 1 continuous hour for a total test duration of not less than 1.5 continuous hours. The administrator and maintenance director discussed deficient items at the exit conference.
Plan of correction · submitted by the facility
Corrective Action takenThe annual polarity retention audit has been scheduled for 8/14/2026. Systemic Changes The Continuing Care Director has educated the Senior Facility Manager and CC Maintenance Supervisor of the NFPA requirement: that receptacles must be tested every 12 months by confirming the correct polarity of hot and neutral wire connections and the retention force of the grounding blade for each electrical receptacle. Monitoring PlanThe monitoring procedure to ensure the PoC is effective and the specific deficiency cited remains corrected and/or in compliance with the regulatory requirements is, the Senior Facility Manager and/or designee will review completion of receptacle inspections to ensure it was completed timely and accurately and to ensure timely follow-up is corrected if identified. Maintenance Supervisor and/or designee will report results to QAPI annually.
6/16/2026Complaint, Recertification Survey · ID 235202-H12 deficiencies▼
0000INITIAL COMMENTSSurveyor note2 building records▼
Findings · record 1 of 2
A recertification survey with Incident #3032909, Incident #3032966 and Incident #3033058 and was conducted on 6/10/26 to 6/16/26. Two deficiencies were cited.
Findings · record 2 of 2
An Emergency Preparedness survey was conducted from 6/10/26 to 6/16/26. No deficiencies were cited.
Plan of correction
The state did not require a plan of correction for this citation.
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 (#3) of one resident reviewed for dialysis out of 25 sample residents. Specifically, the facility failed to:-Ensure thorough dialysis documentation was in place for Resident #3; and,-Ensure staff consistently and thoroughly completed the dialysis communication forms between the facility and the dialysis center for Resident #3. Findings include:I. Facility policy and procedureThe Dialysis policy, revised May 2021, was provided by the nursing home administrator (NHA) on 6/16/26 at 9:00 a.m. It read in pertinent part, “The facility will establish a process for residents who require dialysis to receive services, consistent with professional standards of practice, the comprehensive person-centered care plan and the resident’s goals and preferences. “The facility will create a communication book for each resident who is receiving dialysis. The dialysis communication worksheet accompanies the resident during each dialysis visit to enhance communication. Prior to dialysis, the worksheet will be completed by the licensed nurse or designee of the community which will indicate the current status of the resident. The dialysis team will review the worksheet completed by the licensed nurse or designee prior to dialysis and record pertinent information on the worksheet at the end of the dialysis treatment. Upon return of the resident to the community, the licensed nurse or designee will review the worksheet and follow up on any concerns written by the dialysis team. Any identified concerns/changes in condition documented on the worksheet will be reported to the medical provider.”II. Resident #3A. Resident statusResident #3, age greater than 65, was admitted on 7/24/25. According to the June 2026 computerized physician orders (CPO), diagnoses included end stage renal disease and dependence on renal dialysis (process to filter wastes from the body). The 5/29/26 minimum data set (MDS) assessment revealed the resident was cognitively intact with a brief interview for mental status (BIMS) score of 15 out of 15. He was independent with most activities of daily living (ADL). He had impairment of one lower extremity, he used a walker and wheelchair for mobility, and he required supervision and set up assistance for bathing. The MDS assessment indicated the resident received hemodialysis treatment. B. Record reviewReview of Resident #3’s dialysis care plan, initiated 6/1/26, revealed the resident received dialysis three times weekly and had a right upper extremity fistula (surgically created dialysis access site). Interventions included avoiding performing procedures on the resident’s right arm, coordinating medication administration, weights, and lab results with the dialysis center and monitoring the resident’s dialysis access site for complications and signs of infection. -However, the care plan did not include the dialysis center’s contact information, the resident’s chair time (time spent at dialysis), the transportation company’s contact information, or pre- and post-dialysis treatment instructions. -Review of Resident #3’s June 2026 CPO revealed no physician’s orders related to dialysis. Review of Resident #3’s dialysis communication forms for the month of May 2026 and June 2026 revealed the following:-The 5/1/26, 5/6/26, 5/8/26, 5/11/26, 5/13/26, 5/20/26, 5/22/26, 5/27/26, 6/3/26, 6/5/26, 6/8/26, and 6/10/26 dialysis communication forms were not signed by the nurse upon his return to the facility. -The resident’s weight was marked as N/A (not applicable) on the 5/6/26 form. -No weight was documented in the pre-dialysis section on the 5/20/26 form. -The nurse that completed the pre-dialysis section on the 6/3/26 form did not sign it. -An undated dialysis communication form did not include pre-dialysis vital signs or a weight and was not signed by the nursewhen the resident returned to the facility.-Review of the vital signs and nursing progress notes on Resident #3’s dialysis days in May 2026 and June 2026 revealed no nursing progress notes were documented pre- or post-dialysis. Vital signs were documented pre-dialysis but no vital signs were documented post-dialysis. III. Staff interviews Registered nurse (RN) #2 was interviewed on 6/11/26 at 11:00 a.m. RN #2 said when a resident returned from dialysis, the nurse was to obtain a set of vital signs, assess the resident’s fistula site for bleeding and check for adequate blood flow by listening and feeling the site. She said the nurse was to review the dialysis communication binder to see if the dialysis center documented any new orders or if anything pertinent happened during the resident’s dialysis treatment. The NHA was interviewed on 6/11/26 at 3:00 p.m. The NHA acknowledged that the dialysis communication forms for Resident #3 lacked the needed documentation the facility nurse should complete when a resident returned from a dialysis appointment, such as vital signs, assessing the dialysis access site, and the overall condition of the resident. She said nursing pre- and post-dialysis progress notes were not being completed. Licensed practical nurse (LPN) #2 was interviewed on 6/16/26 at 8:30 a.m. LPN #2 said prior to a resident going to dialysis, the nurse was to complete the pre-dialysis section on the dialysis communication form. She said the nurse was to obtain the resident’s weight and vital signs. She said any medications the resident took during the day while at dialysis were to be sent with the resident for dialysis staff to administer. She said if a resident was out of the facility through meal time, food was sent with them. She said Resident #3 would eat breakfast before he left the facility and snacks were sent with him. LPN #2 said Resident #3 would eat dinner upon returning to the facility. She said a pre-dialysis nursing note should be entered that documented the resident's condition prior to dialysis. She said upon the resident's return to the facility, the nurse was to check the dialysis communication form for any new orders or important information from dialysis, obtain vital signs, a weight, and check the fistula site to ensure adequate blood flow and document all findings in a post-dialysis progress note. RN #1 was interviewed on 6/16/26 at 8:37 a.m. RN #1 said prior to a resident going to dialysis, the nurse was to complete the pre-dialysis communication form that included the resident's weight, vital signs, any medications given, and the fistula site condition. She said the nurse was to document a pre-dialysis progress note that included the resident’s condition information prior to dialysis. She said when the resident returned from the dialysis appointment, the nurse was to check the communication form for any new orders or pertinent information from the dialysis center, obtain vital signs, a weight, and assess the dialysis fistula site for bleeding and adequate blood flow and enter a post-dialysis progress note. She said there were no physician’s orders for nursing to monitor the status of Resident #3's fistula site on a daily basis. The NHA and the director of nursing (DON) were interviewed together on 6/16/26 at 1:00 p.m. The NHA said Resident #3 was the first dialysis resident they had had in the facility in 10 years. She said he transferred to long-term care last year from assisted living and the dialysis orders were not adequate. She agreed the dialysis communication form the facility had been using did not include all the needed information, and nursing staff were not completing all required documentation pre- and post-dialysis. The DON said nursing staff had not been completing all the needed information on the post-dialysis communication form and they were not documenting progress notes before or after Resident #3’s dialysis appointments. She said nursing staff had not been documenting their assessments of the resident's fistula sight for adequate blood flow on a daily basis. She agreed it was important for the fistula to be assessed every day and not just on dialysis days. IV. Facility follow upOn 6/16/26 at 9:00 a.m. the NHA provided the following:A copy of a new dialysis communication form that included the post-dialysis nursing documentation needed when a resident returned from a dialysis appointment, such as vital signs and instructions for the nurse to enter a post-dialysis progress note that included the resident’s condition and assessment of the fistula site. A copy of dialysis care education provided to nursing staff that started on 6/12/26 (during the survey) and was completed on 6/16/26. The education included the new dialysis communication form with required information, fistula site assessment, and reporting any issues to dialysis. The education additionally included examples of how to write a pre- and post-dialysis progress note. Thirteen nursing staff attended the education. A copy of Resident #3's updated care plan that included the addition of the resident’s chair time, and the dialysis center and the transportation company’s contact information. Additional instructions added to the care plan included to complete the dialysis communication form to send with the resident and upon return review the form for any new orders from the dialysis center. Vital signs were to be obtained and the fistula site was to be assessed. An updated physician’s order that indicated Resident #3’s dialysis days, the pick up time, and the dialysis center's contact information, as well as copies of completed dialysis communications forms, dated 6/12/26 and 6/15/26, and the pre- and post-dialysis nursing progress notes on those dates.-However, above changes were not implemented until the concern was brought to the facility’s attention during the survey.
Plan of correction · submitted by the facility
Tag 0698 DialysisCorrective action takenContinuing Care Hemodialysis Communication Worksheet updated to include vital signs post dialysis on 6/12/26. Resident #3’s care plan updated to include dialysis center’s contact information, the resident’s chair time (time spent at dialysis), the transportation company’s contact information, and pre- and post-dialysis treatment instructions on 6/15/26. Physician order for dialysis obtained on 6/15/26. Identification of other residents having the potential to be affectedThere were no additional residents affected by deficient practice as Resident #3 is the only resident on dialysis services at this time. Systemic changesDirector of Nursing and/or designee will review with all nurses the community “Dialysis” policy and “Dialysis Care education.” This includes proper communication and with dialysis facility, nursing documentation, nursing signature of communication forms upon return to facility and physician orders. Dialysis policy review will be added into our new nurse orientation as well as our annual skills review/competency. Monitoring Plan As a measure of ongoing compliance, the Director of Nursing and/or designee will audit 50% of all dialysis communication sheets with vital signs, nursing signature and weight entry weekly for one (1) month and monthly for two (2) months. As a measure of ongoing compliance, the Director of Nursing and/or designee will audit 50% of all pre and post dialysis nursing notes weekly for fistula assessment for one (1) month and monthly for two (2) months. As a measure of ongoing compliance, the Director of Nursing and/or designee will audit 100% of all residents receiving dialysis services for physician order, and care plan to include: dialysis center’s contact information, the resident’s chair time (time spent at dialysis), the transportation company’s contact information, and pre- and post-dialysis treatment instructions monthly for three (3) months. The results of the audits will be reviewed at quality assurance performance improvement (QAPI) monthly for three months to ensure that substantial compliance has been achieved and maintained or for further review/ recommendations. Monitoring will be documented on a spreadsheet. Completion Date: 7/15/26
0880Infection Prevention & Control▼
Findings
Based on observations and interviews, the facility failed to maintain an infection control program designed to provide a safe, sanitary, and comfortable environment to help prevent the development and transmission of diseases and infection on two of four halls. Specifically, the facility failed to:-Ensure staff performed hand hygiene during medication pass; -Ensure medications were administered in a sanitary manner;-Ensure vital signs equipment was sanitized between resident use;-Ensure respiratory equipment was stored in a sanitary manner; and,-Ensure infection control practices were followed during wound care. Findings include:I. Medication pass failuresA. Facility policy and procedureThe Medication Administration policy, revised October 2023, was provided by the nursing home administrator (NHA) on 6/16/26 at 11:48 a.m. It read in pertinent part, “Medications are administered in accordance with nursing standards of practice and state law. Medication will be administered using appropriate infection control and prevention practices.”B. ObservationsOn 6/15/26 at 8:30 a.m. licensed practical nurse (LPN) #1 was observed preparing medications to administer to Resident #44, who was seated at a dining room table. LPN #1 did not perform hand hygiene prior to preparing the medications. LPN #1 placed the medication cup containing several tablets on the dining room table then bumped the cup and caused it to spill two tablets onto the table. She started to pick the medications up with her hand but then used the plastic spoon she had used to administer the medications to the resident and scooped the tablets onto the spoon. LPN #1 placed the two medications back into the medication cup. She then used the same spoon and placed the medications into Resident #44’s mouth. LPN #1 returned to her medication cart and began to prepare Resident #12’s medications. -LPN #1 failed to perform hand hygiene after administering Resident #44’s medications and prior to dispensing Resident #12’s medications into a medication cup and administering them to the resident. C. Staff interviewsLPN #1 was interviewed on 6/15/26 at 9:00 a.m. LPN #1 said that when the medication tablets landed on the dining room table, she should have discarded them and dispensed new tablets. She said she was supposed to sanitize her hands between administering medications to multiple residents but failed to do so. The director of nursing (DON) was interviewed on 6/15/26 at 11:00 a.m. She said LPN #1 should have discarded the medications that landed on the dining room table and dispensed new medications. She said nurses were to sanitize their hands between residents when administering medications. D. Facility follow upOn 6/16/26 at 11:48 a.m. the NHA provided documentation of an inservice, started on 6/15/26 (during the survey) and completed on 6/16/26, with nursing staff on medication administration and infection control policy reminders. Seventeen staff members attended the inservice. The education read,“Wash hands or use hand sanitizer before and after administration of medications. If a medication is dropped onto any surface during administration, that medication should be disposed of and a new medication pulled.”-However, the education was not provided until the concern was brought to the facility’s attention during the survey. II. Equipment failuresA. Facility policy and procedureThe Infection Prevention and Control Safe and Sanitary Environment policy, revised August 2025, was provided by the NHA on 6/16/26 at 11:48 a.m. It read in pertinent part,“To maintain a safe and sanitary environment through the cleaning and disinfection of environmental surfaces as well as the equipment routinely used by residents. The type and frequency of cleaning required for a piece of equipment is dependent on the principles of cleaning and disinfecting surfaces and equipment and takes into account the intended use of the equipment in patient care and the potential of contamination. Non-critical itemsare those items that touch a resident's intact skin, (stethoscopes, blood pressure cuffs, pulse oximeters). Clean these items with a hospital grade disinfectant labeled as tuberculocidal (destroys tuberculosis bacteria).”B. ObservationsOn 6/10/26 at 9:00 a.m. portable oxygen canisters were observed sitting on the floor outside of room #1117 and room #1118. On 6/15/26 at 7:15 a.m. portable oxygen canisters were observed sitting on the floor outside of room 31101, room #1112 and room #1121. On 6/15/26 at 10:00 a.m. registered nurse (RN) #1 was observed obtaining blood pressures on two unidentified residents with the blood pressure cuff touching their bare arms. RN #1 placed a pulse oximeter on their fingers to obtain oxygen saturations and used a stethoscope that was hanging on the vital signs machine to listen to the residents’ lung sounds. She did not sanitize the equipment in between the two residents, even though sanitizing wipes were readily available in the basket of the vital signs machine. On 6/15/26 at 10:15 a.m. a continuous positive air pressure (CPAP) mask was observed lying on top of Resident #43’s bedside table behind the CPAP machine and between the telephone and a lamp base. It was not stored in a sanitary manner, even though a plastic storage bag for the mask was hanging from the top drawer pull of the bedside table. C. Staff interviewThe DON was interviewed on 6/16/26 at 11:48 a.m. The DON said CPAP masks were to be cleaned, air dried, and placed in a bag when not in use, and portable oxygen canisters were not to be placed on the ground. She said vital signs equipment was to be cleaned between resident use with the disinfecting wipes provided on the machines. She said the certified nurse aides (CNA) were interviewed and they said they placed the oxygen canisters on the floor as a reminder to refill them. D. Facility follow upOn 6/16/26 at 11:48 a.m. the NHA provided documentation of an inservice, started on 6/15/26 (during the survey) and completed on 6/16/26, with nursing staff on equipment cleaning and CPAP and oxygen. Seventeen staff members attended the inservice. The education read,“CPAP tubing and masks should be rinsed using mild soap and water after use (in the morning) and allowed to air dry. Place mask and tubing in bag when dry and not in use. Portable oxygen tanks should not be placed on the ground. After use, vital signs equipment should be cleaned with Oxyvir (disinfectant), including the vital signs machine, the blood pressure cuff, and any probes.”-However, the education was not provided until the concern was brought to the facility’s attention during the survey. III. Wound care failureA. Facility policy and procedureThe Skin Integrity Program policy, revised November 2025, was provided by the NHA on 6/16/26 at 11:48 a.m. It read in pertinent part,“When an alteration in skin integrity is present, an interdisciplinary and comprehensive approach will be taken to provide necessary care and treatment to promote healing and prevent infection. The approach to the management of skin injuries and preventions will be consistent with professional standards of practice to promote healing, prevent infection, and prevent new injuries from developing.”B. ObservationsOn 6/15/26 at 1:30 p.m. LPN #1 was observed completing wound care for Resident #16. LPN #1 gathered the wound care supplies that were in a plastic container and placed them within easy reach. She donned (applied) the appropriate personal protective equipment (PPE), which included a gown, gloves, and eye protection. After removing the old dressing from the resident’s wound, she removed her gloves, performed hand hygiene and donned clean gloves. She then cleaned the wound per the physician’s order and placed the bottle of wound cleanser on the floor. After cleaning the wound, LPN #1 removed her gloves, performed hand hygiene, and donned clean gloves. She opened a package that contained a foam dressing that would cover the wound. She then opened a package of silver alginate (antimicrobial bandage), cut it to fit the wound, and wearing the same gloves, she reached under the gown she was wearing and retrieved a black marker from the pocket of her uniform top. LPN #1 used the marker and dated the foam dressing. She then used the same hand that she used to retrieve the marker with to place the piece of silver alginate into the wound bed and covered it with the foam dressing.-LPN #1 failed to change her gloves and perform hand hygiene after retrieving a marker from her uniform top prior to finishing Resident #16’s wound dressing change. C. Staff interviewsLPN #1 was interviewed on 6/15/26 at 2:00 p.m. LPN #1 acknowledged that she should not have reached into her pocket to retrieve the marker and then continued to complete the wound care without removing those gloves, performing hand hygiene, and donning clean gloves. She agreed that no wound care supplies should be placed on the floor. She said normally she would have all the supplies she needed in place for the wound care prior to starting the dressing change. The DON was interviewed on 6/16/26 at 11:00 a.m. The DON said the nurse should gather all the wound care supplies needed prior to starting a wound treatment dressing change so there would not be any breaks in infection control during the wound treatment. The DON said if additional supplies were needed during the wound care, the nurse’s PPE was to be changed. She said no wound care supplies should be placed on the floor. D. Facility follow up On 6/16/26 11:48 a.m. the NHA provided documentation of an inservice, completed on 6/15/26, with nursing staff on infection control and wound care. Seventeen nursing staff members attended the inservice. The education read,“When providing wound care, ensure that all supplies are gathered prior to starting. If additional supplies are needed, PPE must be removed, hands washed, additional items gathered, hands washed, then PPE reapplied.”-However, the education was not provided until the concern was brought to the facility’s attention during the survey.
Plan of correction · submitted by the facility
Tag 0880 Infection Prevention and ControlCorrective action takenSignage placed on vital sign machines (4) on 6/15/26 to “Clean After Use.”Bracket for cleaning wipes placed on two vital sign machine carts that did not previously have them on 6/15/26. LPN (licensed practical nurse) #1 identified during survey for failure to follow infection control practices during wound care and failure to administer medications in a sanitary manner was educated on hand hygiene during medication administration as well as procedure to destroy and pull a new medication if dropped on 6/15/26. CPAP (continuous positive air pressure) mask cleaned for resident #43 on 6/15/26. Identification of other residents having the potential to be affected100% audit of CPAP masks completed to ensure proper storage bag provided and masks cleaned on 6/15/26. One additional resident was identified as utilizing a CPAP machine and potentially affected by the deficient practice. Audit completed on 7/2/26 on 100% of portable oxygen canisters for cleanliness and proper storage. Ten residents that utilize portable oxygen have the potential to be affected by deficient practice. All residents have the potential to be affected by deficiencies in the following practices: Hand hygiene performed during medication pass, Medications administered in a sanitary manner, and vital signs equipment sanitized between use. Systemic changesDirector of Nursing and/or designee will educate all nurses on the “Medication Administration, Receipt, Storage, and Disposal” policy. Director of Nursing or designee will educate all direct care staff on the “Infection Prevention and Control Safe and Sanitary Environment” policy and the “Respiratory Equipment” SOP (standards of practice). Education specific to portable oxygen storage and CPAP cleaning and storage will be added into our new nurse and CNA (certified nurse aide) orientation as well as our annual skills competency. Monitoring Plan As a measure of ongoing compliance, the Director of Nursing and/or designee will audit 100% of all current CPAP masks in use weekly for one (1) month and monthly for two (2) months to check for proper cleaning and storage in the morning after use. Discrepancies will be promptly corrected. As a measure of ongoing compliance, the Director of Nursing and/or designee will audit 10 observations weekly for one (1) month and monthly for two (2) months of staff obtaining vital signs to ensure equipment was properly cleaned after use. Discrepancies will be promptly corrected. As a measure of ongoing compliance, the Director of Nursing and/or designee will complete audit 5 random observations of proper infection control being followed during wound care. This will occur weekly for one (1) month and monthly for two (2) months. As a measure of ongoing compliance, the Director of Nursing and/or designee will audit 10 random medication passes weekly for one (1) month and monthly for two (2) months to observe for medications administered in a sanitary manner including hand hygiene and medication handling. As a measure of ongoing compliance, the Director of Nursing and/or designee will complete environmental rounds on all resident care areas to ensure portable oxygen tanks are stored properly when not in use 2 times weekly for one (1) month and monthly for two (2) months. The results of the audits will be reviewed at quality assurance performance improvement (QAPI) monthly for three (3) months to ensure that substantial compliance has been achieved and maintained or for further review/ recommendations. Monitoring will be documented on a spreadsheet. Completion Date: 7/15/26
1/27/2026Complaint Survey · ID 1E2272-H1No deficiencies▼
0000INITIAL COMMENTSSurveyor note▼
Findings
A survey for Incident #2695762 and Incident #2714896 was conducted on 1/26/26 to 1/27/26. No deficiencies were cited.
Plan of correction
The state did not require a plan of correction for this citation.
6/4/2025Complaint Survey · ID VE8711No deficiencies▼
0000INITIAL COMMENTSSurveyor note▼
Findings
A complaint survey, prompted by #CO39871 was conducted on 6/4/25. No deficiencies were cited.
Plan of correction
The state did not require a plan of correction for this citation.
1/27/2025Complaint Survey · ID H42S11No deficiencies▼
0000INITIAL COMMENTSSurveyor note▼
Findings
A complaint survey, prompted by #CO38850 was conducted on 1/23/25 to 1/27/25. No deficiencies were cited.
Plan of correction
The state did not require a plan of correction for this citation.
10/14/2024Revisit: Recertification Survey · ID UIFD22No deficiencies▼
0000INITIAL COMMENTSSurveyor note▼
Findings
A document revisit was completed with all deficiencies being corrected. No other deficiencies were cited and no response is needed.
Plan of correction
The state did not require a plan of correction for this citation.
9/26/2024Revisit: Recertification Survey · ID UIFD12No deficiencies▼
0000Initial CommentsSurveyor note▼
Findings
A revisit survey was completed on 9/26/24 for all previous deficiencies cited on 8/15/24. The facility is in compliance with all regulations surveyed.
Plan of correction
The state did not require a plan of correction for this citation.
8/29/2024Recertification Survey · ID UIFD216 deficiencies▼
0000INITIAL COMMENTSSurveyor note▼
Findings
INITIAL COMMENTS (ID Prefix Tag #K000) are informational only and represent the facility's general characteristics. This survey was conducted in accordance with the Federal Register at Section 42 CFR 483.70(a). The facility occupies the first floor of a three-story, Type II (222) construction. The facility is protected by a National Fire Protection Association (NFPA) 13 automatic fire suppression system and is classified as Fully Sprinkled. Floors two (2) and Three (3) are occupied by an Assistant Living (Large Board and Care) occupancy. The facility was constructed in 2013 and is licensed for 44 beds. This re-certification survey, conducted on August 29, 2024, was conducted to comply with the National Fire Protection Association (NFPA 101) Life Safety Code (2012) "Chapter 19, Existing Health Care Occupancies". The deficiencies cited were discussed with the Administrator and Maintenance Director during the exit conference conducted at the exit conference.
Plan of correction
The state did not require a plan of correction for this citation.
0131Multiple OccupanciesS/S E▼
Findings
Based on observation and staff interviews during the survey, it was determined that the facility failed to maintain firewalls in accordance with NFPA 101, 8.3.1.2. Fire foam on penetration. Main electrical room. It is not an approved fire-stopping system. NFPA 101, 8.3.1.2 Fire barriers shall comply with one of the following:(1) The fire barriers are continuous from outside wall to outside wall or from one fire barrier to another, or a combination thereof, including continuity through all concealed spaces, such as those found above a ceiling, including interstitial spaces.(2) The fire barriers are continuous from outside wall to outside wall or from one fire barrier to another, and from the floor to the bottom of the interstitial space, provided that the construction assembly forming the bottom of the interstitial space has a fire-resistance rating not less than that of the fire barrier. This deficiency has the potential to affect occupants, who might include residents, staff, and visitors throughout the facility. The maintenance Director discussed deficient items at the exit conference.
Plan of correction · submitted by the facility
Tag 0131: Fire Foam Corrective Action takenThe fire foam has been removed on 9/11/24 by contracted vendor. Approved fire caulking has been applied to effected penetrations on 9/11/14 in main electrical room. Systemic Changes All fire penetrations have been audited to ensure proper fire caulking is applied in all penetrated walls. The General Services Director and/or designee will educate maintenance team and any future vendors or contractors to inform of approved fire caulking procedures for penetrations. Monitoring PlanContinuing Care Maintenance Supervisor and/or designee will audit all penetrations weekly in environmental rounds for 30 days, followed by monthly for 60 days. Results will be documented in audit tool. Results of environmental rounds will be reported to QAPI monthly for 90 days for further interventions or monitoring as indicated.
0222Egress DoorsS/S E▼
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. 1. The therapy patio needs one motion lock, and the exit sign
2. The therapy exit door to the patio needs a sign. NFPA 101 7.2.1.5.10.2 The releasing mechanism shall open the door leaf with not more than one releasing operation unless otherwise specified in 7.2.1.5.10.3, 7.2.1.5.10.4, or 7.2.1.5.10.6. Life Safety Code 19.2.10.1. Means of egress shall have signs in accordance with section 7.10. The directional indicator shall be located outside of the Exit legend, not less than 3/8 in. (1cm) from any letter. The directional indicator shall be of a chevron type. The directional indicator shall be identifiable as a directional indicator at a distance of 40 ft. (12.2m). A directional indicator larger than the minimum established in this paragraph shall be proportionately increased in height, width, and stroke. The directional indicator shall be located at the end of the sign for the direction indicated. This deficiency could affect occupants, including residents, staff, and visitors within the entire facility. Deficient items were discussed with the administrator and maintenance director at the exit conference.
Plan of correction · submitted by the facility
Tag 0222: Egress DoorsCorrective Action takenThe community has added signs on internal patio door and external patio gate indicating “emergency exit“ on 9/11/24. Single motion lock has been installed on patio gate on 9/9/24. Systemic Changes A house wide audit of all egress doors was completed to ensure appropriate signage is in place with correct locks. The General Service Director and/or designee will educate Security and Emergency Services Managers and maintenance personnel on applying appropriate exit signs to egress doors. Monitoring PlanContinuing Care Maintenance Supervisor and/or designee will audit all exit signs weekly in environmental rounds for 30 days, followed by monthly for 60 days. Results will be documented in audit tool. Environmental rounds will be reported to QAPI monthly for 90 days for further interventions or monitoring as indicated.
0353Sprinkler System - Maintenance and TestingS/S E▼
Findings
Through observation during the documentation review, it was determined that the facility failed to meet the protection requirements in accordance with NFPA 101, 25, and 13. The linen closet pipe needs to be switched to black iron, not CPVC mechanical, and the janitor closet needs to be changed. Painted sprinkler stairwell 1 6.3.6.2 Pipe or tube listed for light hazard occupancies shall be permitted to be installed in ordinary hazard rooms of otherwise light hazard occupancies where the room does not exceed 400 ft2 (37 m2). 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. This deficiency can potentially affect occupants, including residents, staff, and visitors within the entire facility. Deficient items were discussed with the administrator and maintenance director at the exit conference.
Plan of correction · submitted by the facility
Tag 0353: Sprinkler System Corrective Action takenThe CPVC piping has been removed and replaced with black iron piping in the linen closet and housekeeping/janitor closet on 9/6/24. The sprinkler head in stairwell 1 was removed and replaced on 9/3/24. Systemic Changes The General Services Director and/or designee will educate maintenance team on regulation 6.3.6.2 and NFPA 25 5.2.1.1.2 to ensure awareness of sprinkler head and piping compliance standards. Monitoring PlanContinuing Care Maintenance Supervisor and/or designee will audit all sprinkler heads and piping weekly in environmental rounds for 30 days, followed by monthly for 60 days. Results will be documented in audit tool. Results of environmental rounds will be reported to QAPI monthly for 90 days for further interventions or monitoring as indicated.
0354Sprinkler System - Out of ServiceS/S D▼
Findings
Based on observations and records review, it was determined that the facility did not have Sprinkler System out-of-service guidance in accordance with NFPA 101 and NFPA 25Fire sprinkler out of service | need correct verbiage NFPA 101, 9.7.6 Sprinkler impairment procedures shall comply with NFPA 25, Standard for the Inspection, Testing, and Maintenance of Water-Based Fire Protection Systems. NFPA 25, 15.5.2 Before authorization is given, the impairment coordinator shall be responsible for verifying that the following procedures have been implemented:(1) The extent and expected duration of the impairment have been determined.(2) The areas or buildings involved have been inspected and the increased risks determined.(3) Recommendations have been submitted to management or the property owner or designated representative.(4) Where a required fire protection system is out of service for more than 10 hours in a 24-hour period, the impairment coordinator shall arrange for one of the following:(a) Evacuation of the building or portion of the building affected by the system out of service(b) *An approved fire watch(c)*Establishment of a temporary water supply(d)* Establishment and implementation of an approved program to eliminate potential ignition sources and limit the amount of fuel available to the fire(5) The fire department has been notified.(6) The insurance carrier, the alarm company, property owner or designated representative, and other authorities having jurisdiction have been notified.(7) The supervisors in the areas to be affected have been notified.(8) A tag impairment system has been implemented. (See Section 15.3.)(9) All necessary tools and materials have been assembled on the impairment site. This deficiency has the potential to affect occupants, who might include residents, staff, and visitors throughout the facility. The administrator and maintenance director discussed deficient items at the exit conference.
Plan of correction · submitted by the facility
Tag 0354: Sprinkler System Corrective Action takenReview of fire watch policy completed and was determined that policy is more stringent than code regulation. Policy indicates that any fire safety system impairment will trigger fire watch at 4 hours, which would include a sprinkler system impairment (rather than 10 hours as indicated in fire code). Specifically, the policy describes that a fire safety/ life safety system includes, “fire suppression sprinkler system“, “stand pipe system“ and “fire alarm system.“The procedure further outlines:In the event that facility personnel are informed of a planned period where the fire/ life safety systems will be out of service for 4 hours or more, or in the event of failure of the fire / life safety systems where they appear they may be out of service for a period of 4 hours or more, Fire Watch procedures will be implemented. However, the policy has been updated to provide further clarity. Specifically, that if fire alarm system or life safety system, including fire suppression sprinkler system, stand pipe system or fire alarm is out of service for four (4) hours or more, a fire watch will be implemented. This exceeds the NFPA required 10 hours or more. Systemic ChangesSecurity and Emergency Services Manager or designee will provide education with competency to all security and maintenance staff to ensure adequate understanding of our policy and definition of a fire watch. Monitoring PlanThe Security and Emergency Services Manager or designee will perform a random audit of five (5) security and maintenance staff to ensure continued understanding and knowledge competency of our fire watch policy. This will be achieved through staff members being able to appropriately answer:- What is a fire watch?- What situations would entail a fire watch?- What is our policy regarding when to implement a fire watch?This audit will occur monthly for three (3) months and presented to QAPI Committee for further interventions or monitoring as indicated.
0712Fire DrillsS/S D▼
Findings
Based on the record review, it was determined that the facility failed to conduct fire drills in accordance with the Life Safety Code, Section 19.7.1.6Fire drills closer than an hour apart, not at varied timesNFPA 101, 19.7.1.6 Drills shall be conducted quarterly on each shift to familiarize facility personnel (nurses, interns, maintenance engineers, and administrative staff) with the signals and emergency action required under varied conditions. This deficiency could affect occupants, including residents, staff, and visitors within the entire facility. Deficient items were discussed with the administrator and maintenance director at the exit conference.
Plan of correction · submitted by the facility
Tag 0712: Fire DrillsCorrective Action takenThe community has updated the master schedule of all fire drills to ensure all drills are scheduled at least one hour apart and are not repeated times throughout the 12 month cycle. A repeat drill is scheduled to be completed on 9/13/24 at 8:00AM.Systemic Changes The Security and Emergency Manager and/or designee will educate and inform staff to conduct fire drills at unexpected times and under varying conditions, and to ensure drills are kept on planned schedule to avoid repeated times. Monitoring PlanAll fire drill reports will be submitted to the Security and Emergency Manager and/or designee to ensure: all scheduled drills occurred according to schedule. Results of each fire drill will be reported to QAPI monthly for 90 days for further interventions or monitoring as indicated. Fire drill master schedule has been updated as of 8/30/24. The next fire drill is scheduled for 10/8/24 at 6:52pm.
0914Electrical Systems - Maintenance and TestingS/S F▼
Findings
Based on the documentation review, it was determined that the facility did not maintain proper electrical practices in accordance with NFPA 99 Health Care Facilities Code (2012). This was evidenced by:1. No written record of the continuity of the grounding circuit, polarity of hot and neutral connections, and retention force of the grounding blade in patient care rooms was conducted annually. 2. Gfci near sink nurse station kitchen. NFPA Standard: NFPA 99 Health Care Facilities Code (2012)6.3.3.2 Receptacle Testing in Patient Care Rooms. 6.3.3.2.1 The physical integrity of each receptacle shall be confirmed by visual inspection. 6.3.3.2.2 The continuity of the grounding circuit in each electrical receptacle shall be verified. 6.3.3.2.3 Correct polarity of the hot and neutral connections in each electrical receptacle shall be confirmed. 6.3.3.2.4 The retention force of the grounding blade of each electrical receptacle (except locking-type receptacles) shall be not less than 115 g (4 oz). NFPA 70 550.13 Receptacle Outlets.(A) Grounding-Type Receptacle Outlets. All receptacle outlets shall comply with the following:(1)Be of grounding type(2)Be installed according to 406.4(3)Except where supplying specific appliances, be 15- or 20-ampere, 125-volt, either single or multiple type, and accept parallel-blade attachment plugs(B) Ground-Fault Circuit Interrupters (GFCI). All 125-volt, single-phase, 15- and 20-ampere receptacle outlets installed outdoors, in compartments accessible from outside the unit, or in bathrooms, including receptacles in luminaires, shall have GFCI protection. GFCI protection shall be provided for receptacle outlets serving countertops in kitchens and receptacle outlets located within 1.8 m (6 ft) of a wet bar sink. The exceptions in 210.8(A) shall be permitted. This deficiency has the potential to affect occupants, who might include residents, staff, and visitors throughout the facility. The maintenance director discussed deficient items at the exit conference.
Plan of correction · submitted by the facility
Tag 0914: Electrical SystemsCorrective Action takenOn 8/29/24, Senior Facilities Manager completed 100% audit of all electrical receptacles in skilled nursing for polarity and retention force. No polarity issues found. Receptacles with retention force concerns have been adjusted to be above the 8oz threshold. Previous receptacle near bistro sink was removed and replaced with GFCI receptacle on 9/11/24. Systemic Changes Senior Facility Manager will educate general services team on annual requirement of testing for polarity and retention force and the need for retention force to be above 8oz. The inspection has been scheduled annually with General Services Team to be completed by Maintenance Supervisor and/or designee. If any concerns are found with polarity or retention force, they will be corrected immediately. Monitoring PlanThe monitoring procedure to ensure the PoC is effective and the specific deficiency cited remains corrected and/or in compliance with the regulatory requirements. Senior Facility Manager or designee will review completion of inspection to ensure it was completed timely and completely. Senior Facility Manager or designee will complete a visual inspection of 35% of total receptacles each month for 90 days and report findings to QAPI monthly. Maintenance Supervisor or designee will report results to QAPI annually.
8/15/2024Recertification Survey · ID UIFD111 deficiency▼
0000Initial CommentsSurveyor note2 building records▼
Findings · record 1 of 2
A recertification survey was conducted on 8/12/24 to 8/15/24. One deficiency was cited.
Findings · record 2 of 2
An Emergency Preparedness survey was conducted from 8/12/24 to 8/15/24. No deficiencies were cited.
Plan of correction
The state did not require a plan of correction for this citation.
0761Label/Store Drugs and BiologicalsS/S D▼
Findings
Based on observations, record review and interviews, the facility failed to ensure all drugs and biologicals were labeled and stored properly according to professional standards in two of five locked cabinets in resident rooms. Specifically, the facility failed to ensure medications were labeled with the date they were opened. Findings include:I. Professional referenceAccording to the manufacturer Astra Zeneca, Symbicort Medication Guide (June 2024), retrieved on 8/19/24 from https://den8dhaj6zs0e.cloudfront.net/50fd68b9-106b-4550-b5d0-12b045f8b184/a4b62ab8-1314-4583-91b4-294ec239f790/a4b62ab8-1314-4583-91b4-294ec239f790_pi_med_guide_rendition__c.pdf, "Throw away Symbicort when the counter reaches zero or three months after you take Symbicort out of its foil pouch, whichever comes first."According to the manufacturer NovoNordisk, Storage and Travel with Tresiba (June 2024), retrieved on 8/19/24 from https://www.mynovoinsulin.com/insulin-products/tresiba/how-to-take-tresiba/flextouch-storage.html, "Storage after use - dispose after eight weeks, even if there is insulin left in the pen or vial and the expiration date has not passed."According to the manufacturer NovoNordisk, Taking Novolog-Insulin Aspart (March 2023), retrieved on 8/19/24 from https://www.mynovoinsulin.com/insulin-products/novolog/taking-novolog.html, "Storage after use - keep at room temperature or refrigerated up to 28 days. Dispose after 28 days, even if there is insulin left in the pen or vial."II. Facility policy and procedureThe Storage and Expiration Dating of Medications and Biologicals policy, revised August 2024, was provided by the director of nursing (DON) on 8/15/24 at 2:45 p.m. The policy read in pertinent part,"Once any medication or biological package is opened, the facility should follow manufacturer/supplier guidelines with respect to expiration dates for opened medications. "Facility staff should record the date opened on the primary medication container (example vial, bottle, inhaler) when the medication has a shortened expiration date once opened."III. Observations and interviewsOn 8/14/24 at 1:58 p.m., the medication storage cabinet in Resident #17's room was observed with licensed practical nurse (LPN) #2. The following was observed:-An opened Tresiba Flex Touch U-100 insulin pen was not labeled with the date it was opened for use. -An opened Novolog U-100 insulin pen was not labeled with the date it was opened for use. LPN #2 said the insulin pens should have been labeled when opened. LPN #2 said she did not know what the facility policy said about the storage of insulin pens. LPN #2 said she would check with the staff from the previous shift to find out if they knew when the insulin pens were opened. -LPN #2 did not remove the insulin pens from Resident #17's medication storage cabinet. On 8/15/24 at 10:27 a.m., the medication storage cabinet in Resident #4's room was observed with LPN #1. The following was observed:-An opened Symbicort 160 microgram (mcg)/4.5 mcg inhaler was not labeled with the date it was opened for use. LPN #1 said inhalers should be labeled with a date the medication was opened. LPN #1 said she did not know if inhalers could be used until the manufacturer expiration date after they were opened. IV. Staff interviewsRegistered nurse (RN) #2 was interviewed on 8/13/24 at 2:00 p.m. RN #2 said the residents' medications were stored in the residents' rooms in locked cabinets. She said the facility did not have medication carts. The DON was interviewed on 8/14/24 at 2:15 p.m. The DON said insulin pens should be labeled with the date they were opened and staff should know how long the pens could be opened before they needed to be discarded. The DON said the Tresiba and Novolog insulin pens needed to be discarded and she would immediately discard the insulin pens and replace them with new pens which would be labeled with the date they were opened. The DON said she planned to check all staff competencies and confirm appropriate education had been provided. The DON said that insulin could be less effective if not discarded by the recommended disposal date. The DON was interviewed a second time on 8/15/24 at 11:04 a.m. She said inhalers should be labeled with the date they were opened. The DON said staff should check manufacturers' instructions for information about when inhalers needed to be discarded when opened. The DON said inhalers could be less effective if used beyond the recommended disposal date. V. Facility follow-upOn 8/14/24 at 2:48 p.m, the DON provided a staff education document titled Insulin Pen Storage/Dating. The education contained three staff signatures and was dated 8/14/24 (during the survey). The education content included adding the date opened to medication vials when put in use and expiration dates of medications after opening. The document included reference to a second document provided without a title which described storage information specific to Tresiba and Novolog. The document revealed Tresiba should be discarded eight weeks after opening and Novolog Flex Pens should be discarded 28 days after opening. The DON said the information was posted in Resident #17's medication storage cabinet.
Plan of correction
The state did not require a plan of correction for this citation.
1/22/2024Focused Infection Control, Other-Fed Survey · ID N848111 deficiency▼
0884Reporting - National Health Safety NetworkS/S F▼
Findings
Based on record review, the facility failed to report complete information about COVID-19 to the Centers for Disease Control and Prevention's (CDC) National Healthcare Safety Network (NHSN) during a seven-day period that reporting was required by regulation. The CDC submitted data from the NHSN to the Centers for Medicare and Medicaid Services (CMS). Based on review of that data, CMS determined that between 01/15/2024 and 01/21/2024, the facility did not report complete information to NHSN about COVID-19 in the standardized format and frequency as specified by CMS and the CDC. This failure to report has the potential to cause more than minimal harm to all residents residing in the facility.
Plan of correction
The state did not require a plan of correction for this citation.
Reportable Occurrences
18 records6/9/2026Brain Injury · ID 2602H136005Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 6/9/26, 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 brain injury event. Client (A) suffered an unwitnessed fall from bed resulting in facial injuries. Client (A) was transferred to the hospital for further evaluation. Diagnostic test results revealed a brain bleed and client (A) was admitted. During the course of the investigation, the healthcare entity conducted a post fall review, record review and interviews. The facility concluded the fall was accidental and occurred when client (A) attempted to adjust their bed height. Once medically cleared, client (A) returned. Staff reassessed client (A)'s safety needs, updated the plan of care, and re-educated the client on the mechanics of bed controls. 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 7/7/2026 · released to the public 7/20/2026.
3/28/2026Physical Abuse · ID 2602H136004Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 3/28/26, 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 physical abuse event. While staff (1) responded to client (A)'s call light, client (A) alleged staff (2) abused them by pushing them around, yanking and pulling on them. Client (A) indicated they felt staff (2) handled them aggressively and reported being scared staff (2) could potentially hurt them. Staff (2) entered the room and was redirected to leave. During the course of the investigation, the healthcare entity suspended staff (2), conducted an assessment and interviews, notified the police and implemented a supportive and safety monitoring plan for the client. No visible injury was observed with client (A), but they expressed experiencing pain during the interactions. Staff (2) reported client (A) did not require too much physical assistance and denied the allegations. No other clients reported having a concern with staff (2) or being handled in a rough manner. Staff acknowledged the client utilizes their call light frequently and has shown signs of increased confusion surrounding their care needs and environment. A medication review occurred with client (A) and they were referred for mental health support. Staff (2) returned to work. 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 6/22/2026 · released to the public 6/29/2026.
3/24/2026Neglect · ID 2602H136003Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 3/25/26, 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 neglect event. Client (A) reported they were experiencing pain the previous night, and allegedly staff (1) did not administer their requested as needed pain medications in a timely manner. Client (A) also brought up concerns about staff (1)'s professionalism with a follow-up interaction, which caused them to feel fearful. During the course of the investigation, the healthcare entity suspended staff (1), conducted an assessment and interviews, and reviewed records. Client (A) reported they did receive their pain medications from staff (1) seventy minutes after their initial request. Staff (1) reported being behind with passing medications that night and denied the allegation of being unprofessional. No other clients or staff reported having concerns about staff (1)'s professionalism or medication administration. The facility concluded staff (1) did not intentionally withhold medication but management acknowledged the delivery of pain medication had been late. Staff requested a medication review for client (A)'s pain. Additional education and training was provided to staff (1) regarding time management, administrative support and their customer service approach. A neglect 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 6/23/2026 · released to the public 6/30/2026.
3/12/2026Physical Abuse · ID 2602H136002Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 3/12/26, 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 physical abuse event. Client (A) alleged a caregiver employed with an outside agency had "beat her up" while providing care. Client (A) alleged the caregiver handled her in a rough manner causing pain and did not feel safe working with the caregiver. During the course of the investigation, the healthcare entity requested the caregiver leave and notified their agency. Nursing conducted an assessment, which showed no visible injuries, but client (A) reported having mild pain. Management notified the police. Through additional interviews, client (A) said the caregiver provided a bath, which did not follow client (A)'s plan of care to have a second person present for support and safe handling. The caregiver denied providing a bed bath but said they assisted with incontinence care. The caregiver indicated client (A) did not convey any complaint of pain. The facility concluded the caregiver moved the client alone without having a second facility staff member person present, which deviated from client (A)'s plan of care. The agency caregiver was removed from working with this client and agency staff received education on client (A)'s plan of care. According to conflicting interviews, an abuse event could not be 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 5/22/2026 · released to the public 6/4/2026.
3/1/2026Verbal Abuse · ID 2602H136001Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 3/3/26, 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 verbal abuse event. Client (A) alleged a staff person (staff 1) leaned in close to their face and told him they were using the call light too much. Client (A) initially reported feeling threatened and scared for their safety. Client (A) could not recall the specific timeframe or name the staff person. During the course of the investigation, the healthcare entity provided reassurance to client (A), conducted interviews, and notified the police. Management reviewed call light reports, staffing assignments and suspended staff matching client (A)'s description. Staff (1) and other staff reported client (A) does use the call light frequently but denied the allegation that they said anything to the client. No other clients reported concerns with safety. Client (A)'s medication and medical needs were reassessed due to noted confusion and a recent behavioral change. Staff (1) returned to work. The facility took the opportunity to review support strategies to use with client 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 5/21/2026 · released to the public 5/29/2026.
11/18/2025Physical Abuse · ID 2502H136007Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 11/17/25, 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 a physical abuse event. Client (B) alleged staff provided care in a rough manner and did not stop when asked. During the course of the investigation, the healthcare entity conducted an assessment and interviews, suspended staff, notified the police and implemented a supportive and monitoring plan. No visible injury was observed, and client (B) denied having more pain. Later, client (B) indicated staff were not actually rough, but they changed her when she did not want to be changed. Prior to returning to work, the identified staff received education regarding listening to clients’ right to refuse care. Staff requested a medication review for client (B) due to her chronic pain and signs of increased anxiety with 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 1/22/2026 · released to the public 1/29/2026.
10/25/2025Neglect · ID 2502H136006Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 10/25/25, the healthcare entity investigated a reportable event of neglect. Reportedly, staff heard client (A) claim she was going to kill herself and then observed client (A) cutting one wrist with a butter knife. Staff intervened to remove the knife. Client (A) had been successful in making superficial cuts to her wrist, and first aid was provided until the paramedics arrived. Client (A) was transported to the hospital and admitted. During the course of the investigation, the healthcare entity conducted interviews, reviewed records and checked the environment for any harmful items. Records showed client (A) had a history of suicidal ideation and former attempts. However, through the facility’s current assessments and from staff interviews, client (A) did not exhibit signs of active suicidal thoughts or make any current comments about harming self-prior to this incident. Client (A) did not return to this facility, as she transferred to another setting to help with her mental health needs. There were no findings of staff neglect with this unfortunate event. 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 1/27/26, Event ID 1E2272-H1.
Publication
Sent to facility 2/19/2026 · released to the public 2/26/2026.
10/18/2025Brain Injury · ID 2502H136005Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 10/19/25, 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 a brain injury event. Staff observed client (A) on the floor with a bump on the back of her head. Client (A) was transported to the hospital where diagnostic test results showed two brain bleeds. Client (A) was admitted for medical care and monitoring due to a functional change. During the course of the investigation, the healthcare entity conducted a post fall review, record review and interviews. The facility concluded the client (A) did not call for staff help and fell while attempting to walk to the restroom. Client (A) remained in the hospital. 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 1/6/2026 · released to the public 1/13/2026.
8/19/2025Physical Abuse · ID 2502H136004Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 8/21/25, 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 a physical abuse event. Client (B) alleged staff (1) handled her in a rushed and reckless manner, which caused her pain. During the course of the investigation, the healthcare entity suspended staff (1), conducted an assessment and interviews, notified the police and implemented a supportive and safe monitoring plan. No visible injury was observed with client (B). Staff (1) said they did move client (B)’s legs abruptly, which caused pain, but denied being reckless. Later client (B) said she did not think staff (1)’s actions were done with intent. Management concluded staff (1) deviated from the client’s mobility plan of care. The allegation of abuse was not substantiated. However, due to a reported pattern of customer service concerns and performance issues, management terminated staff (1)’s employment. All care staff received re-education on ensuring care was provided in a manner that was not perceived as rushed. 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 11/6/2025 · released to the public 11/13/2025.
7/28/2025Physical Abuse · ID 2502H136003Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 7/28/25, 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 a physical abuse event. Reportedly, staff noticed a physical change with client (B)’s hand/wrist area. X-ray reports showed a fracture to one of the client’s wrist bones, which was an injury of unknown origin. During the course of the investigation, the healthcare entity conducted an assessment, interviews, record review and notified the police. The age of the fracture was indeterminant and a positioning device was applied. With client (B)’s cognitive impairment, she was unable to participate in a follow up interview about a potential cause of injury. Through the facility findings, the cause of injury could not be determined, and an abuse allegation could not be substantiated or unsubstantiated. Staff received reminders about her plan of care needs. 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 10/29/2025 · released to the public 11/5/2025.