Respiratory Equipment Not Dated or Stored per Policy
Summary
The facility did not ensure that residents receiving respiratory care had oxygen and nebulizer equipment managed in accordance with facility policy and professional standards. During the recertification survey, surveyors identified deficiencies for two of three residents reviewed for oxygen administration: one resident’s oxygen tubing was not dated or labeled to show when it had been changed, and another resident’s nebulizer tubing was not dated or labeled to show when it had been changed and the nebulizer mask was not stored in a plastic bag when not in use. Resident #48 was admitted with diagnoses including acute infarction of the intestine, hypertension, and hypoxemia. The resident’s MDS dated 7/31/2025 documented that the resident could be understood by others and was cognitively intact. Facility policy stated oxygen cannula tubing was to be changed weekly and as needed. On observations on 8/8/2025 and 8/11/2025, the resident was receiving oxygen via nasal cannula at 2 liters per minute, and the tubing had no date to reflect when it had been changed. The July and August 2025 MARs/TARs did not document an order to change the tubing per facility policy, and progress notes from 7/25/2025 through 8/18/2025 contained no documentation of an oxygen tubing change. Resident #163 was admitted with diagnoses including type 2 diabetes mellitus, hyperlipidemia, and gastrointestinal hemorrhage. The resident’s MDS documented that the resident could be understood and understand others and had severely impaired cognition for daily living decisions. Facility policy for nebulizer medication stated that after treatment the equipment should be rinsed, disinfected, washed, air dried, and stored in a plastic bag with the resident’s name and date on it, and that tubing should be changed every seven days or according to facility protocol. On multiple observations in August 2025, the nebulizer mask was found on top of the nightstand rather than in a plastic bag, and the tubing was not labeled with a date. The resident was ordered ipratropium-albuterol solution by nebulizer twice daily, but the MAR/TAR did not document when the nebulizer tubing was changed, and staff interviews indicated they were unsure when the tubing had last been changed.
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