Respiratory equipment was not handled or documented according to orders
Summary
Safe and appropriate respiratory care was not maintained for residents receiving oxygen and nebulizer therapy. For Resident #24, surveyors observed unbagged, undated nasal cannula tubing attached to a portable oxygen tank in the wheelchair pocket, with the prongs touching the wheelchair surface. The resident stated he/she used oxygen continuously and used the portable tank often when leaving the room. Nursing staff stated the portable oxygen was applied when the resident transferred to the wheelchair, but the tubing was later observed draped behind the concentrator with the nasal cannula touching the floor while the concentrator was off. RN #3 then picked up the tubing and placed the cannula in the resident’s nose after it had been in contact with the floor, and the oxygen flow was observed set at 2.5 L/min even though the order was for 1-2 L/min. Resident #35’s nebulizer tubing and mouthpiece were observed stored on top of the resident’s bed, with the mouthpiece in direct contact with papers and later with bed linens. The resident had an active order for ipratropium-albuterol inhalation solution and a separate order to disinfect the nebulizer daily, rinse it, air dry it, and store it in a clean container, but the January 2026 MAR/TAR lacked evidence that the nebulizer was disinfected and stored according to the order. RN #6 stated the mouthpiece should not be stored on the bed and that after use it should be cleaned, air dried, and stored on a surface, but she was not sure exactly how it should be stored. Resident #41’s oxygen concentrator and portable tank were observed with unbagged, undated nasal cannula tubing coiled so the prongs touched the concentrator and the tank surface. The resident stated he/she no longer used the concentrator but sometimes used the tank. The record showed the last documented oxygen use was 11/19/25, and the MAR/TAR showed an oxygen monitoring order that had been discontinued on 12/9/25. For Resident #6, the record showed continuous oxygen use during observation, but the chart lacked a current provider order for oxygen use, and there was no documentation of the amount of oxygen in use or regular oxygen saturation monitoring. The DON acknowledged the lack of a current order and the absence of documentation.
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