20
Inspections
21
Deficiencies
0
Actual Harm or Above
3
Occurrences
July 9, 2026
Last Inspection
S/S D/E/F Potential for harm
The most recent inspection of CENTER AT NORTHRIDGE, LLC, THE on record is dated July 9, 2026. Across 20 published inspections, state surveyors cited 21 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
HAMLER, TROY
Owner
THE CENTER AT NORTHRIDGE, LLC
Phone
(303) 280-4444
Payor Source
Medicare, Private Pay
City
WESTMINSTER
ZIP
80234-3439
Inspections & Citations
20 inspections · 21 deficiencies7/9/2026Complaint, Recertification Survey · ID 25C719-H11 deficiency▼
0000INITIAL COMMENTSSurveyor note2 building records▼
Findings · record 1 of 2
A recertification survey with complaint #CO2636900 and #CO3023236 was completed on 7/6/26 to 7/9/26. One deficiency was cited.
Findings · record 2 of 2
An Emergency Preparedness survey was conducted from 7/6/26 to 7/9/26. No deficiencies were cited.
Plan of correction
The state did not require a plan of correction for this citation.
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 on two of two units. Specifically, the facility failed to:-Ensure staff donned (put on) the appropriate personal protective equipment (PPE) when providing care to Resident #31, who was on enhanced barrier precautions (EBP); -Ensure housekeeping staff followed appropriate infection control guidelines when cleaning residents’ rooms; and, -Ensure Resident #50’s respiratory equipment was properly cleaned and stored. Findings include: I. Failed to ensure staff donned the appropriate PPE when providing care to Resident #31, who was on EBPA. 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) (updated 4/2/24), retrieved on 7/8/26 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.”“Expand the use of PPE and refer to the use of gown and gloves during high-contact resident care activities that provide opportunities for transfer of MDROs to staff hands and clothing. MDROs may be indirectly transferred from resident to resident during these high-contact 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 a gown and gloves for high-contact resident care activities was 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), or wound care (any skin opening requiring a dressing).“In general, gown and gloves would not be required for resident care activities other than those listed above, unless otherwise necessary for adherence to standard precautions. Residents are not restricted to their rooms or limited from participation in group activities. Because enhanced barrier precautions do not impose the same activity and room placement restrictions as contact precautions, they are intended to be in place for the duration of a resident's stay in the facility or until resolution of the wound or discontinuation of the indwelling medical device that placed them at higher risk."B. Facility policy and procedureThe Enhanced Barrier Precautions (EBP) policy, dated 3/27/24 and revised 1/29/25, was received from the nursing home administrator (NHA) on 7/8/26 at 12:44 p.m. The policy read in pertinent part,“To reduce transmission of multidrug-resistant organisms by employing targeted gown and glove use during high-contact resident care activities. Per the CDC, EBPs are recommended (whencontact precautions do not otherwise apply during high-contact care activities with residents who are at higher risk of acquiring or spreading an MDRO. Enhanced barrier precautions include the use of a gown and gloves during the high-contact patient care activities: changing briefs or assisting with toileting.”C. ObservationOn 7/8/26 at 8:42 a.m. physical therapist #1 was assisting Resident #31, who was on EBP, with toileting assistance in the bathroom. The door to the bathroom was ajar. PT #1 was verbalizing his actions to the resident while wiping the resident's backside. The toilet was flushed and PT #1 emerged from the bathroom, only wearing gloves. -PT #1 failed to wear a protective gown while assisting Resident #31 with toileting hygiene. D. Resident interviewResident #31 was interviewed on 7/8/26 at 10:45 a.m. Resident #31 said he was on EBP due to a wound on his foot. E. Staff interviewPT #1 was interviewed on 7/8/26 at 8:49 a.m. PT #1 said Resident #31 was on EBP. He said when assisting a resident with EBP, he should be wearing a gown and gloves. PT #1 said it was important to wear EBP to reduce the risk of transmission of germs from resident to resident. II. Failed to ensure housekeeping staff followed appropriate infection control guidelines when cleaning residents’ roomsA. Facility policy and procedureThe Cleaning Room policy, dated 11/1/17 and reviewed on 3/8/24, was received from the NHA on 7/8/26 at 12:44 p.m. The policy read in pertinent part, “Our team can control the spread of infection by performing daily disinfection and adhering to all hand hygiene protocols. Always work from the cleanest to the dirtiest. Daily routine needs to include high-touch areas, which can include: door knobs, light switch, sharps box, table and tray, call light and phone when not being held by the resident, call box and pull cord, commode seat, rim, and flusher. If you have to leave the room after you have started a room clean, remove your gloves and perform hand hygiene. Put a new pair of gloves on to resume cleaning. “Always use a fresh towel when cleaning a toilet:- Wipe the toilet paper dispenser;- Wipe the flusher;- Wipe the toilet seat;- Wipe under the bowl;- Wipe the toilet rim; and,- Clean the inside of the bowl using disinfectant cleaner and a toilet brush.”The Hand Hygiene policy, dated 12/5/2020 and reviewed 1/7/24, was received from the NHA on 7/8/26 at 12:44 p.m. The policy read in pertinent part, “Soap and water: Use when hands become dirty or soiled. Hand sanitizer: Use an alcohol-based hand sanitizer that contains at least 60% alcohol. Put enough sanitizer on your hands to cover all surfaces. Rub your hands together until they feel dry. Do not rinse or wipe off.”B. ObservationOn 7/7/26 at 2:35 p.m. housekeeper (HK) #1 was observed cleaning room #204. HK #1 donned clean gloves and removed the trash bags from the trash cans and disposed of them. HK #1 then made the bed and folded extra blankets. She donned clean gloves. She got a cleaning rag and germicidal ultra bleach spray from her cart. HK #1 then sprayed the sink and wiped it down with a clean rag. She grabbed the toilet cleaner, dispensed some in the toilet, and used the toilet brush in the bowl, on the rim, and on the bottom of the seat. HK #1 then changed her gloves and got a clean rag to wipe the handrails in the bathroom. -HK #1 failed to perform hand hygiene throughout the entire process of cleaning resident room #204. -HK #1 failed to clean the high-touch areas, such as the door knobs in room #204.-HK #1 failed to clean the toilet from the cleanest area to the dirtiest area. C. Staff interviewsHK #1 was interviewed on 7/7/26 at 2:55 p.m. HK #1 said she forgot to wash her hands when she was cleaning room #204. She said it was important to wash her hands to prevent the spread of germs. HK #1 said that she used the toilet brush to scrub the lid of the toilet. She said she understood that the brush should stay in the toilet bowl and that by bringing the brush out of the toilet bowl and cleaning the toilet seat, bacteria could be transferred. The housekeeping supervisor was interviewed on 7/9/26 at 8:40 a.m. The housekeeping supervisor said she instructed the housekeeping staff to change gloves and sanitize their hands when disposing of a dirty rag. The housekeeping supervisor said that the housekeepers were required to clean the high-touch areas in residents’ rooms on a daily basis. The housekeeping supervisor said the toilet brush should only be used in the toilet bowland the housekeeping staff should follow this rule in order to avoid cross contamination. III. Failed to ensure Resident #50’s respiratory equipment was properly cleaned and storedA. Facility policy and procedureThe Respiratory Equipment policy, dated 9/14/17 and revised on 11/18/25, was received from the NHA on 7/9/26 at 9:07 a.m. The policy read in pertinent part, “Residents will have an order that includes settings when indicated for CPAP (continuous positive airway pressure)/BiPAP (bilevel positive airway pressure).“Respiratory equipment will be cleaned and stored per the manufacturer’s guidelines.”B. ObservationOn 7/8/26 at 10:43 a.m. Resident #50 had her nebulizer mask lying on the bedside table without a paper towel underneath it. The resident's noninvasive portable ventilator was at the bedside with the mask in the basket, not in a bag. On 7/9/26 at 10:55 a.m. Resident #50 was receiving a nebulizer treatment with a new mask; however, there was still a nebulizer mask on the bedside table, not on a paper towel. The resident’s noninvasive portable ventilator was at the bedside, with the mask on top of the machine, not in a plastic bag. C. Resident interviewResident #50 was interviewed on 7/9/26 at 10:14 a.m. Resident #50 said she was on contact precautions due to clostridium difficile (C. diff - a highly contagious bacterium that causes severe inflammation of the colon and watery diarrhea). She said that the nurse did not wash her noninvasive portable ventilator mask yesterday or today after use. Resident #50 said that her other nebulizer mask had also not been washed. D. Staff interviewLicensed practical nurse (LPN) #3 interviewed on 7/9/26 at 11:20 a.m. LPN #3 said she was going to enter Resident #50's room and remove the old nebulizer mask and wash the new mask she had given to the resident today (7/9/26). LPN #3 said she would wash the resident's noninvasive ventilator mask and place it in a plastic bag. She said the importance of cleaning and placing the resident’s respiratory equipment in a clean bag was because the resident had respiratory issues and was on precautions due to C. diff. IV. Additional staff interviewsThe infection preventionist (IP) and the director of nursing (DON) were interviewed together on 7/9/26 at 11:30 a.m. The IP said she conducted re-education with the therapy department about EBP and the importance of adhering to the use of a gown and gloves when performing care with residents on EBP. The DON said that it was the nurses' responsibility to remind the staff when they forgot to use proper PPE when working with residents on EBP. The IP said the housekeeping department was re-educated about the importance of good hand hygiene when removing soiled gloves and donning clean gloves. The DON said nebulizer masks should be rinsed and then air-dried on a paper towel. The DON said there was a plastic bag that the mask would go in until the next use. She said the mask for Resident #50’s portable noninvasive ventilator should be cleaned as the physician's order indicated and placed in a clean plastic bag. The IP said there was a holder that Resident #50’s portable noninvasive ventilator mask should go on after drying. The IP said that it was important to clean the mask to prevent the growth of microorganisms.
Plan of correction · submitted by the facility
Preparation and execution of this response and plan of correction does not constitute an admission of agreement by the provider of the truth of the facts alleged or conclusions set forth in the statement of deficiencies. The plan of correction is prepared and or executed solely because it is required by the provision of the state and federal law. For the purpose of any allegation the facility is not in substantial compliance with Federal requirements of participation, this response and plan of correction constitutes the facility's allegation of compliance in accordance with the State Operations Manual. F 880 SS=D Infection Prevention and Control#1: Corrective Action-Patients AffectedEnhanced Barrier Precautions: Residents #31 was assessed and determined to appropriately be on Enhance Barrier Precautions (EBP). The signage on the patient’s room was also checked and was properly posted. PPE (personal protective equipment) was available outside of the patient’s room. Housekeeping Procedure: Patient in room 204 was no longer in the facility when this POC (plan of correction) was submitted. No patient specific corrective action needed. Respiratory Equipment Cleaning and Storage: Patient #50 was no longer in the facility when we received the 2567. No patient specific corrective action needed.#2: Other Patients AffectedAll patients on Enhanced Barrier Precautions are at a potential risk for this alleged EBP deficient practice. All patients are at a potential risk for the alleged Housekeeping Procedure deficient practice. All patients with respiratory equipment are at risk for the alleged Respiratory Cleaning and Storage deficient practice.#3: Systemic ChangesThe Director of Rehabilitation or designee educated Physical Therapists on the importance of a proper adherence to Enhanced Barrier Precautions. The Environmental Services Director or designee educated housekeeping staff on the proper infection control procedures when cleaning a patient room. The Director of Nursing or designee educated nurses on the proper way to clean and store respiratory equipment.#4: MonitoringThe Director of Rehabilitation or designee will monitor Physical Therapists weekly for 4 weeks to ensure they demonstrate their ability to properly follow the Enhanced Barrier Precaution protocol, then once per month for one month. This monitoring will continue for a total of 90 days or until substantial compliance is achieved. The Environmental Services Director or designee will monitor Housekeepers weekly for 4 weeks to ensure they demonstrate their ability to properly follow the proper room cleaning protocol, then once per month for one month. This monitoring will continue for a total of 90 days or until substantial compliance is achieved. The Director of Nursing or designee will monitor Nurses weekly for 4 weeks to ensure they demonstrate their ability to properly clean and store respiratory equipment, then once per month for one month. This monitoring will continue for a total of 90 days or until substantial compliance is achieved. The monitoring of each element will be tracked on monitoring forms. The NHA (nursing home administrator) will bring the results of the monitoring to QAPI (quality assurance performance improvement) meeting monthly for a minimum of 3 months (longer if needed), until the facility demonstrates substantial compliance with all elements of the alleged deficient practice.
7/9/2026Licensure Complaint Survey · ID 25C782-H1No deficiencies▼
0000Initial CommentsSurveyor note▼
Findings
A survey with #CO3023237 was completed on 7/6/26 to 7/9/26. No deficiencies were cited.
Plan of correction
The state did not require a plan of correction for this citation.
12/4/2025Complaint Survey · ID 1D805B-H1No deficiencies▼
0000INITIAL COMMENTSSurveyor note▼
Findings
A complaint survey, prompted by #CO2599303 was conducted on 9/25/25 to 12/4/2025. No deficiencies were cited. The actual exit date was 9/25/25. Per AHFSA guidance from CMS on 11/17/25, the survey end date has been been adjusted to the date the CMS-2567 was issued to the provider, on 12/4/25.
Plan of correction
The state did not require a plan of correction for this citation.
8/19/2025Complaint Survey · ID GO4W11No deficiencies▼
0000INITIAL COMMENTSSurveyor note▼
Findings
A complaint survey, prompted by #CO1943720 was conducted on 8/19/25. No deficiencies were cited.
Plan of correction
The state did not require a plan of correction for this citation.
6/4/2025Complaint Survey · ID MQJT11No deficiencies▼
0000INITIAL COMMENTSSurveyor note▼
Findings
A complaint survey, prompted by #CO38988 and #CO40033 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.
10/9/2024Complaint Survey · ID YOUB11No deficiencies▼
0000INITIAL COMMENTSSurveyor note▼
Findings
A complaint survey, prompted by #CO37482 and #CO37517 was conducted on 10/8/24 to 10/9/24. No deficiencies were cited.
Plan of correction
The state did not require a plan of correction for this citation.
9/5/2024Complaint Survey · ID YVJC11No deficiencies▼
0000INITIAL COMMENTSSurveyor note▼
Findings
A complaint survey, prompted by #CO37213 and #CO37214 was conducted on 9/3/24 to 9/5/24. No deficiencies were cited.
Plan of correction
The state did not require a plan of correction for this citation.
7/8/2024Revisit: Recertification Survey · ID QUNS22No 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.
5/23/2024Revisit: Recertification Survey · ID QUNS12No deficiencies▼
0000Initial CommentsSurveyor note▼
Findings
A revisit survey was completed on 5/23/24 for all previous deficiencies cited on 4/2/24. The facility is in compliance with all regulations surveyed.
Plan of correction
The state did not require a plan of correction for this citation.
4/25/2024Recertification Survey · ID QUNS2112 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). This survey was conducted on April 25, 2024, for compliance with the National Fire Protection Association, (NFPA 101) Life Safety Code (2012) Chapter 19 "Existing Health Care Occupancies."This structure is a one (3) story, Type II (111) (VA) construction. The facility was constructed in 2016 and has no basement. There are three smoke compartments located on the 1st floor and four smoke compartments located on floors 2 and 3. Emergency power is supplied by a natural gas generator that is located on the roof. Medical gas is not to exceed 20,000 cu. ft. on the first floor and medical gas not to exceed 20,000 cu. ft. in portable O2 within the transfer rooms on the 2nd and 3rd floors. The facility is licensed for 96 beds and the census on the survey date was 85. The facility is fully protected throughout by a National Fire Protection Association (NFPA) 13 automatic wet-pipe fire sprinkler system. The facility is classified as fully sprinkled. The results of this survey were discussed with the Maintenance Director during the exit conference conducted on April 25, 2024.
Plan of correction
The state did not require a plan of correction for this citation.
0222Egress DoorsS/S F▼
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. Delayed Egress doors state delayed egress, but they do not have delayed egress. NFPA 101, 7.2.1.6.1.1 A readily visible, durable sign in letters not less than 1 in. (25 mm) high and not less than 1/8 in. (3.2 mm) in stroke width on a contrasting background that reads as follows shall be located on the door leaf adjacent to the release device in the direction of egress: PUSH UNTIL ALARM SOUNDS DOOR CAN BE OPENED IN 15 SECONDS or PUSH UNTIL ALARM SOUNDS DOOR CAN BE OPENED IN 30 SECONDS (if approved by the local fire department) (3)*An irreversible process shall release the lock in the direction of egress within 15 secondsThis 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
Preparation and execution of this response and plan of correction does not constitute an admission of agreement by the provider of the truth of the facts alleged or conclusions set forth in the statement of deficiencies. The plan of correction is prepared and or executed solely because it is required by the provision of the state and federal law. For the purpose of any allegation the facility is not in substantial compliance with Federal requirements of participation, this response and plan of correction constitutes the facility's allegation of compliance in accordance with the State Operations Manual K-222 Egress Doors- Delayed Egress DoorsPatients AffectedNo patients were directly affected by the incomplete delayed-egress doors. Other Patients AffectedAll patients have the potential to be affected by the incomplete delayed-egress doors. Systemic ChangesThe Maintenance Director or Designee will cover the delayed egress labeling until the Delayed Egress Doors are activated and operable. All delayed egress doors will go through the Division of Fire Protection and Control plan review. Upon completion, the Maintenance Director or Designee will conduct an inspection of all delayed egress doors for 4 weeks, and all delayed egress doors for two months to ensure proper operation. MonitoringThe Maintenance Director will deliver the audit results to the Executive Director upon completion and the Executive Director will bring the results to the QAPI meeting for a minimum of 3 months or until substantial compliance is achieved
0293Exit SignageS/S F▼
Findings
Through observation during the survey, it was determined that the facility failed to meet the exit signage requirements in accordance with NFPA 101, 19.2.10.1. And 7.9 This was evidenced by:There were no exit sign testing records at the time of inspection. 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 betweentests, 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 jurisdictionLife Safety Code Section 19.2.10.1 to comply with 7.10Life Safety Code Section 7.10.9.2 Testing. Exit signs connected to, or provided with, a battery-operated emergency illumination source, where required in 7.10.4, shall be tested and maintained in accordance with 7.9.3. This deficiency can potentially affect occupants, including residents, staff, and visitors throughout the facility. The maintenance director discussed deficient items during the survey and with the maintenance director and Administrator at the exit conference.
Plan of correction · submitted by the facility
K-293 Exit Sign Testing Patients AffectedNo patients were directly affected by the missing exit sign testing documentation. Other Patients AffectedAll Patients, Visitors and Staff have the potential to be affected by the missing exit-sign testing documentation. Systemic ChangesThe Executive Director educated the Director of Maintenance on the importance of monthly exit-sign testing. The Maintenance Director or Designee will complete the appropriate exit-sign testing and document accordingly. MonitoringThe Maintenance Director will deliver the monthly results to the Executive Director upon completion and the Executive Director will bring the results to the QAPI meeting for a minimum of 3 months or until substantial compliance is achieved
0324Cooking FacilitiesS/S F▼
Findings
Based on observation, the facility failed to maintain the kitchen hood suppression system as required by NFPA 96. 1. Semi-Annual Hood Inspection | No report available
2. Semi-Annual Hood Inspection | No report available
3. The kitchen hood doesn ' t report to the fire panel. NFPA 96 11.2.1* Maintenance of the fire-extinguishing systems and listed exhaust hoods containing a constant or fire-activated water system that is listed to extinguish a fire in the grease removal devices, hood exhaust plenums, and exhaust ducts shall be made by properly trained, qualified, and certified person(s) acceptable to the authority having jurisdiction at leastevery 6 months. 11.4* Inspection for Grease Buildup. The entire exhaust system shall be inspected for grease buildup by a properly trained, qualified, and certified person(s) acceptable to the authority having jurisdiction and in accordance with Table 11.4. 11.4 Table Systems serving moderate-volume cooking operations Semiannually10.6.2 Where a fire alarm signaling system is serving the occupancy where the extinguishing system is located, the activation of the automatic fire-extinguishing system shall activatethe fire alarm signaling systemThis 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
K-324 Cooking Facilities – Exhaust Hood Patients AffectedNo patients were directly affected by the missing Exhaust-Hood-Inspection Reports, nor the kitchen hood not communicating with the fire panel. Other Patients AffectedAll patients have the potential to be affected by the missing Exhaust Hood Inspection reports and the kitchen hood not communicating with the fire panel. Systemic ChangesThe Executive Director educated the Maintenance Director on the importance of receiving a report with any/all inspections performed. Also on the importance of timely follow-up on any noted issues on these reports. The Maintenance Director will get the Hood Inspection Company to generate reports with all inspections, and will have an appropriate vendor re-establish communication between the Kitchen Hood and the Fire Panel. MonitoringThe Maintenance Director will deliver the inspection reports and completed work order to the Executive Director. The Executive Director will bring the results to the QAPI meeting for a minimum of 3 months or until the facility reaches substantial compliance.
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 13.1. Escutcheon plates through the building exceed 1/8th clearance. 2. The restroom next to the medical supply room needs a drywall gap filled around the fire sprinkler head. 3. Escutcheon missing freezer. NFPA 25, 5.2.1.1.5 Escutcheons and coverplates for recessed, flush, and concealed sprinklers shall be replaced with their listed escutcheon or coverplate if found missing during the inspection. NFPA 13 6.2.7.1 Plates, escutcheons, or other devices used to cover the annular space around a sprinkler shall be metallic or shall be listed for use around a sprinkler. 8.5.6.4 Where sprinklers penetrate a single membrane of a fire-resistance–rated assembly in buildings equipped throughout with an approved automatic fire sprinkler system, noncombustible escutcheon plates shall be permitted, provided that the space around each sprinkler penetration does not exceed 1/2 in. (13 mm), measured between the edge of the membrane and the sprinkler. This deficiency can potentially affect occupants, including residents, staff, and visitors throughout the facility. The administrator discussed deficient items at the exit conference.
Plan of correction · submitted by the facility
K-353 Sprinkler System – maintenance and testing “escutcheon plates“Patients AffectedNo patients were directly affected by the miss-aligned or missing sprinkler escutcheon plates. Other Patients AffectedAll patients have the potential to be affected by the miss-aligned or missing sprinkler escutcheon plates. Systemic ChangesThe Executive Director educated the Maintenance Director on the importance of properly aligned and intact escutcheon plates. The Maintenance Director or Designee will visually inspect all sprinkler escutcheon plates and adjust or repair as necessary. MonitoringThe Maintenance Director or Designee will visually inspect all sprinkler escutcheon plates monthly to ensure compliance. The Maintenance Director will deliver the inspection report to the Executive Director upon completion. The Executive Director will bring the results to the QAPI meeting for a minimum of 3 months or until the facility reaches substantial compliance.
0363Corridor - DoorsS/S D▼
Findings
Based on observation and staff interviews during the course of the survey, it was determined that the facility failed to maintain corridor doors in accordance with the Life Safety Code Section 19.3.6.3 1. Fire Doors to patient rooms have gaps. Rooms 210 and 215. NFPA 101, 19.3.6.3.1 19.3.6.3.1* Doors protecting corridor openings in other than required enclosures of vertical openings, exits, or hazardous areas shall be doors constructed to resist the passage of smoke. NFPA 101, 19.3.6.3.2, (2) In smoke compartments protected throughout by an approved, supervised automatic sprinkler system in accordance with 19.3.5.7, the door construction materials requirements of 19.3.6.3.1 shall not be mandatory, but the doors shall be constructed to resist the passage of smoke. This deficient practice could affect all residents within the smoke compartments should the egress become untenable, due to smoke and heat transfer via the non-latching corridor doors and gaps in the door smoke seal. Deficient items were discussed with the maintenance director during the survey and the Maintenance Director and Administrator at the exit conference.
Plan of correction · submitted by the facility
K-363 Corridor Doors – Gaps in door sealsPatients AffectedNo patients were directly affected by the gaps in the corridor doors. Other Patients AffectedAll patients have the potential to be affected by the gaps in the corridor doors. Systemic ChangesThe Executive Director educated the Maintenance Director on the importance of properly sealed corridor doors. The Maintenance Director or Designee will repair the door gaps in rooms 210 and 215. MonitoringThe Maintenance Director or Designee will visually inspect corridor door seals monthly to ensure no gaps. The Maintenance Director will deliver the inspection report to the Executive Director upon completion. The Executive Director will bring the results to the QAPI meeting for a minimum of 3 months or until the facility reaches substantial compliance.
0372Subdivision of Building Spaces - Smoke BarrieS/S D▼
Findings
Based on observation and staff interviews during the survey, it was determined that the facility failed to maintain smoke barriers in accordance with NFPA 101, 8.5.1. This was evidenced by the following:IT room needs fire caulk around wires coming through a rated wall. NFPA 101, Section 8.5.1, in part, smoke barriers shall be provided to subdivide building spaces for the purpose of restricting the movement of smoke. This deficiency can potentially affect occupants, including residents, staff, and visitors throughout the facility. The maintenance director discussed deficient items at the exit conference.
Plan of correction · submitted by the facility
K-372 Corrective Action – Smoke Barriers/Wall PenetrationsPatients AffectedNo patients were directly affected by the unsealed wall penetrations around wires penetrating a wall in the IT room. Other Patients AffectedAll patients have the potential to be affected by the unsealed wall penetrations around wires penetrating a wall in the IT room. Systemic ChangesThe Maintenance Director or Designee will patch all unsealed penetrations in the IT room. The Maintenance Director will educate all maintenance and housekeeping staff on the importance of intact smoke barriers and the need for immediate reporting of any found penetrations of these barriers, to the Maintenance Director or Executive Director. The Maintenance Director or Designee will conduct a full inspection of all electrical rooms to ensure no additional smoke barriers have open penetrations. MonitoringThe Maintenance Director will deliver the educations and audit results to the Executive Director upon completion and the Executive Director will bring the results to the QAPI meeting for a minimum of 3 months or until substantial compliance is achieved
0521HVACS/S F▼
Findings
Based on observation and staff interviews, it was determined that the facility failed to maintain smoke dampers in accordance with Life Safety Code Section NFPA 105Records were unavailable at the time of the survey to document the inspection and testing operation of the fire dampers. NFPA 105, 6.5.1 Smoke dampers for dedicated and non-dedicated smoke control systems shall be inspected and tested in accordance with NFPA 92A, Standard for Smoke-Control Systems Utilizing Barriers and Pressure Differences. 6.5.2* Each damper shall be tested and inspected one year after installation. The test and inspection frequency shall then be every 4 years, except in hospitals, where the frequency shallbe every 6 years. 6.5.3 Care shall be exercised that all tests are completed in a safe manner wearing the appropriate personal protective equipment. 6.5.4 Full unobstructed access to the damper shall be verified and corrected as required. This deficiency can potentially affect occupants, including residents, staff, and visitors throughout the facility. The administrator discussed deficient items at the exit conference.
Plan of correction · submitted by the facility
K-521 HVAC – Smoke Damper Inspection and Testing DocumentationPatients AffectedNo patients were directly affected by the missing Smoke-Damper Inspection and Testing documentation. Other Patients AffectedAll patients have the potential to be affected by the missing Smoke-Damper Inspection and Testing documentation. Systemic ChangesThe Executive Director educated the Maintenance Director on the importance of receiving and keeping available Smoke Damper Inspection and Testing documentation. The Maintenance Director or Designee contacted Inspection Company that completed the Smoke Damper Inspection and Testing on February 28th 2022 and had them send the facility a copy of the report. This report and all supporting documentation are now available in the Maintenance Director’s office. MonitoringThe Maintenance Director or Designee will continue to obtain Smoke Damper Inspections every 4 years and will maintain these inspection reports in a binder readily available for inspection. The Executive Director will bring the results to the QAPI meeting for a minimum of 3 months or until the facility reaches substantial compliance
0712Fire DrillsS/S F▼
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 19.7.1.6Only 2 fire drills were conducted throughout the last twelve months. NFPA 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 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
K-712 Fire Drills – Patients Affected No patients were directly affected by the lack of fire drill testing. Other Patients AffectedAll patients have the potential to be affected by the lack of fire drill testing. Systemic ChangesThe Executive Director educated the Maintenance Director on the importance of conducting fire drills on an appropriate quarterly schedule. The Maintenance Director or Designee will create a fire drill schedule that meets the requirement and will conduct the drills as per the schedule. The Maintenance Director will record the drills on the schedule. This report and all supporting documentation will be available in the Maintenance Director’s office. MonitoringThe Maintenance Director or Designee will conduct fire-drill testing quarterly on each shift at varying times. The Maintenance Director will record and deliver the reports of the drills to the Executive Director. The Executive Director will bring the results to the QAPI meeting for a minimum of 3 months or until the facility reaches substantial compliance.
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: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. 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). This deficiency can potentially affect occupants, including residents, staff, and visitors throughout the facility. The maintenance director discussed deficient items at the exit conference.
Plan of correction · submitted by the facility
K-914 Electrical Systems – Outlet testingPatients AffectedNo patients were directly affected by the lack electrical outlet testing. Other Patients AffectedAll patients have the potential to be affected by the lack electrical outlet testing. Systemic ChangesThe Executive Director educated the Maintenance Director on the importance of appropriate electrical outlet testing. The Maintenance Director or Designee will test all electrical outlets and record the results of the test. They will continue to test them annually as per code. This report and all supporting documentation will be available in the Maintenance Director’s office. MonitoringThe Maintenance Director or Designee will test all electrical outlets as required and will deliver the results to the Executive Director. The Executive Director will bring the results to the QAPI meeting for a minimum of 3 months or until the facility reaches substantial compliance.
0918Electrical Systems - Essential Electric SysteS/S F▼
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. Missing: Annual Test Annually NFPA 110-8.4 Operational Inspection and Testing. 8.4.1* EPSSs, including all appurtenant components, shall be inspected weekly and exercised under load at least monthly. A.8.3.5 Where sealed devices are used, replacement of the complete device might be necessary. Maintenance should be performed according to manufacturer ' s recommendations. Inthe absence of such recommendations, the list given in 8.3.5 suggests minimal procedures. Transfer switches should be subjected to an annual maintenance program including (one) major maintenance and (three) quarterly inspections. Programs should include all of the following operations. Note: Due to the critical nature of these devices, permission should be gained toperform these tasks since some of the following recommendations could cause disruption of power to the load. The following tasks should be carefully reviewed with facility management personnel to ensure agreement and plan for contingenciesThis deficiency can potentially affect occupants, including residents, staff, and visitors throughout the facility. The maintenance director discussed deficient items at the exit conference.
Plan of correction · submitted by the facility
K-918 Electrical Systems – Generator TestingPatients AffectedNo patients were directly affected by the alleged lack of documentation of annual testing of the backup generator. Other Patients AffectedAll patients have the potential to be affected by the alleged lack of documentation of annual testing of the backup generator. Systemic ChangesThe Executive Director educated the Maintenance Director on the importance of completing and recording this annual backup generator test. MonitoringThe Maintenance Director or designee will outsource to a qualified person an appropriate annual generator test. The Maintenance Director will deliver the results of this test to the Executive Director. The Executive Director will deliver these results to the monthly QAPI committee for a minimum of three months or until substantial compliance is achieved.
0920Electrical Equipment - Power Cords and ExtensS/S D▼
Findings
Through observation during the survey, it was determined that the facility failed to meet the healthcare facilities code requirements in accordance with NFPA 99 and NEC 70. This was evidenced by: 1) power strip supplying power to a refrigerator in the salon officeFlexible 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 the occupants, who might include the residents, staff, and visitors within affected smoke compartments. The maintenance staff and facility administrator discussed deficient items during the exit conference.
Plan of correction · submitted by the facility
K-920 Electrical Equipment – Power cords and Extension CordsPatients AffectedNo patients were directly affected by the alleged improper use of a power strip. Other Patients AffectedAll patients have the potential to be affected by the alleged improper use of a power strip. Systemic ChangesThe Executive Director educated the Salon Manager on the importance of appropriate use of a power strip. The Executive Director moved the mini-fridge and plugged it directly into an appropriate wall outlet. MonitoringThe Maintenance Director or Designee will monitor the Salon for proper usage of power strips monthly. The Maintenance Director will deliver these results to the Executive Director monthly. The Executive Director will bring the results to the QAPI meeting for a minimum of 3 months or until the facility reaches substantial compliance.
0923Gas Equipment - Cylinder and Container StoragS/S E▼
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: 1 The cylinder needs to be labeled/separated by empty and full. 2 Improper storage of oxygen cylinders in soiled linen and therapy support rooms. 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. NFPA 99: .11.3.2* Storage for nonflammable gasses greater than 8.5 m3 (300 ft3), but less than 85 m3 (3000 ft3), at STP shall comply with the requirements in 11.3.2.1 through 11.3.2.3.11.3.2.1 Storage locations shall be outdoors in an enclosure or within an enclosed interior space of noncombustible or limited-combustible construction, with doors (or gates outdoors) that can be secured against unauthorized entry. This deficiency can potentially affect occupants, including residents, staff, and visitors within the entire facility. Deficient items were identified during the survey and discussed with the Administrator at the exit conference.
Plan of correction · submitted by the facility
K-923 Gas Equipment – Cylinder and Container StoragePatients AffectedNo patients were directly affected by the alleged improper storage of oxygen cylinders. Other Patients AffectedAll patients have the potential to be affected by the alleged improper storage of oxygen cylinders. Systemic ChangesThe Executive Director educated the Management Team on the importance of proper storage of portable Oxygen Cylinders. The Maintenance Director posted signs indicating the all Oxygen Cylinders be stored in the Oxygen Exchange room; and labeled and separated between “empty“ and “full“. All portable oxygen containers were moved the appropriate location. MonitoringThe Maintenance Director or Designee will monitor the facility for proper storage of portable oxygen cylinders. The Maintenance Director will deliver these results to the Executive Director monthly. The Executive Director will bring the results to the QAPI meeting for a minimum of 3 months or until the facility reaches substantial compliance.
Reportable Occurrences
3 records6/5/2025Misappropriation of Property · ID 2502I148002Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 6/5/25, 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 misappropriation of property event. Client (B) reported $30 was missing. During the course of the investigation, the healthcare entity conducted a search and interviews, reminded client (B) of the options available in the facility to secure her items and notified the police. Client (B)’s family claimed the client had money in her possession at the facility. However, the client did not disclose she had money in her possession at the facility, and it was not secured. Management was unable to identify an alleged assailant or determine what might have happened, so the 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 9/4/2025 · released to the public 9/11/2025.
9/3/2023Sexual Abuse · ID 2302I148003Reported on time: Yes▼
Occurrence summary
DESCRIPTION OF OCCURRENCE:
On 9/3/23, a resident, in her 70s, made an initial allegation of sexual assault saying she had been touched inappropriately during two therapy sessions. During one interaction, she recalled sliding down in her wheelchair, which prompted the staff member to hug her from behind with their arms beneath her breasts and lifting her back into a proper seating position. She indicated understanding the reason behind their actions, but she believed the staff member enjoyed it too much. The following day, she alleged the staff member touched her right breast in a sexual manner four times when she was lying in bed. The door had been open, and when she asked the staff member to leave, they left.
FACILITY / AGENCY ACTION:
The facility conducted an internal investigation and notified the police, family/guardian, and physician. Emotional support was provided. Management suspended the staff member pending investigation. Management requested female caregivers work with the resident. During a follow up interview, the resident clarified the first encounter was incidental. With the second encounter, she now said her breast was not touched. It was more the collar bone/upper chest area. Staff discovered the resident was a victim of past sexual abuse. The staff member acknowledged the need to reposition the resident in the wheelchair to prevent a fall but denied any inappropriate touching with each interaction. With the second encounter, the staff member said they touched her hand when trying to convince her to participate in therapy. No other residents or staff reported having any concerns about the staff member’s professionalism. The facility concludes the incidents described by the resident were not sexual abuse. Mental health services was offered. Education was provided to the staff member regarding best strategies to encourage patient participation when they are reluctant to participate in needed therapy services. The staff member returned to work.
DEPARTMENT FINDINGS:
In accordance with Colorado Revised Statute 25-1-124, the Department conducted an off-site investigation of this reportable event and investigative findings submitted by the agency/facility. This public summary is based on information provided by the agency/facility to the Occurrence Section of the Department and is accurate and complete at this time. Prior to the next onsite investigation of the agency/facility, this occurrence will be reviewed.
The occurrence report indicated the agency/facility acted appropriately in response to this occurrence by complying with licensing standards of reporting and investigating this occurrence.
Publication
Sent to facility 11/22/2023 · released to the public 11/29/2023.
1/26/2023Verbal Abuse · ID 2302I148001Reported on time: Yes▼
Occurrence summary
DESCRIPTION OF OCCURRENCE:
On 1/26/23, a family member contacted the facility to report an allegation of abuse. A resident, in her 80s, alleged a staff member told her that her children hated her and alleged the staff member threatened to strangle her while she slept. Emotional support was provided to the resident. The facility reported the resident had a severe cognitive impairment. With her diagnoses, the facility staff noted she was experiencing a rapid decline of her cognitive, medical and physical status. During a follow up interview with social services, the version of the story changed.
FACILITY / AGENCY ACTION:
The facility conducted an internal investigation and notified the police, physician, and family. Management suspended the staff member pending investigation. A nurse assessed the resident and no adverse findings were noted. Staff reported she was not exhibiting signs of distress or fear. The staff member denied the allegations. No other residents voiced having concerns about this staff member. From the facility findings, the facility was unable to substantiate or unsubstantiated the resident’s allegations. Management implemented care in pairs to ensure there were no unwitnessed interactions. The staff member returned to work but was reassigned not to work with this resident.
DEPARTMENT FINDINGS:
In accordance with Colorado Revised Statute 25-1-124, the Department conducted an off-site investigation of this reportable event and investigative findings submitted by the agency/facility. This public summary is based on information provided by the agency/facility to the Occurrence Section of the Department and is accurate and complete at this time. Prior to the next onsite investigation of the agency/facility, this occurrence will be reviewed.
The occurrence report indicated the facility/agency acted appropriately in response to this occurrence by complying with licensing standards of reporting and investigating this occurrence.
Publication
Sent to facility 6/30/2023 · released to the public 6/30/2023.