Respiratory equipment not cleaned, dated, or stored properly
Summary
The facility failed to promote cleanliness and help prevent the spread of infection related to respiratory care equipment for seven residents who used oxygen or nebulizer therapy. Facility policies required oxygen concentrator water bottles to be changed weekly, concentrators to be cleaned when soiled, nasal cannulas to be replaced every seven days and stored in plastic bags when not in use, and small volume nebulizer equipment to be rinsed, dried, dated, and stored in labeled bags with tubing replaced every seven days. Resident R7 had diagnoses including dementia, kidney disease, heart failure, and type 2 diabetes, and had an order for DuoNeb via nebulizer every six hours. On observation, the resident’s nebulizer mask was dated 5/11/26 and was lying on the bedside stand, not stored in a plastic bag. Resident R24 had COPD, depression, shortness of breath, a suicide attempt, and anxiety, and had an order for oxygen at 2 lpm as needed. On observation, the resident’s oxygen tubing with nasal cannula was lying across the bed and was not stored in a plastic bag. Resident R31 had respiratory failure, COPD, heart failure, and pleural effusion, with orders for oxygen at 2 lpm continuously and DuoNeb twice daily; the nebulizer mask was lying on the bedside table, and the oxygen tubing with nasal cannula was lying on the wheelchair seat and was not stored in a plastic bag. Resident R41 had COPD, irregular heartbeat, heart failure, and respiratory failure, with an order for oxygen at 3 lpm via nasal cannula continuously at bedtime; the oxygen tubing with nasal cannula was lying over the top of the concentrator and was not stored in a plastic bag. Resident R75 had COPD, irregular heartbeat, dementia, and atherosclerotic heart disease, with an order for oxygen as needed to keep saturation above or equal to 92%; the most recent documented oxygen use was months earlier, yet the oxygen tubing was still dated, lying over the concentrator, the humidifier bottle was empty, and the concentrator cannister was covered in dust. Resident R87 had COPD, heart failure, atherosclerotic heart disease, and peripheral vascular disease, with oxygen ordered as needed; the oxygen tubing with nasal cannula was lying on top of the concentrator, the external cannister was dusty, and the humidifier bottle was empty. Resident R155, newly admitted with COPD, stroke, atherosclerotic heart disease, and sleep apnea, had an order for ipratropium bromide four times daily, and the nebulizer mask was lying on the bed, not dated, and not stored in a plastic bag. The NHA and DON confirmed the equipment was not changed timely and should have been stored in a plastic bag when not in use, and that R75’s oxygen concentrator and tubing should have been removed from the room, cleansed, and placed in storage.
Penalty
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