Medication Labeling, Discontinued Medications, and Vaccine Refrigerator Monitoring
Summary
The facility failed to ensure drugs and biologicals were labeled in accordance with accepted standards when Resident 69’s fluticasone/salmeterol inhaler dispenser and insulin aspart injectable pen were observed without the resident’s name and medication expiration date on the dispenser and without an expiration date on the injectable pen. During the observation, the LVN obtained the inhaler and insulin pen from the medication storage area and entered the resident’s room with them. The resident’s record showed diagnoses including type 2 diabetes mellitus, atrial fibrillation, acute kidney failure, shortness of breath, and cough. The LVN stated the inhaler dispenser and insulin syringe could have been mixed up with another resident’s medication and that the resident could have been given the wrong medication. The DON also stated the insulin pen and inhaler were not labeled appropriately and should have had their own labels to ensure the medication was given to the right resident and was not expired. The facility also failed to remove discontinued medications from active medication and treatment carts for multiple residents. Resident 57’s hydrocodone-acetaminophen blister packet remained in the medication cart even though the order had ended on 3/1/26. Resident 155’s clotrimazole cream remained in the treatment cart after the resident had been discharged and the medication had been discontinued. Resident 45’s nystatin topical powder and clotrimazole cream were found in the treatment cart even though the orders had ended, and Resident 19’s collagenase ointment and silver sulfadiazine cream were observed in the treatment cart, including duplicate tubes with labels showing prior start and end dates and opened dates. Staff interviews confirmed these medications were discontinued, and the DON stated discontinued medications should have been removed from the carts and placed in the medication room to avoid being given to residents. The facility further failed to monitor the temperature of the medication refrigerator containing vaccines two times per day. During observation, the refrigerator in the medication room contained shingles vaccine vials, and RN 1 stated the temperature was monitored once daily. The temperature log showed entries for the refrigerator and room temperatures, but the log did not reflect the twice-daily monitoring described in the facility’s vaccine temperature recording form. The DON stated the refrigerator temperatures for the vaccine storage unit were not monitored appropriately and that staff should have checked and documented the refrigerator temperature twice a day, once in the morning and once before the end of the workday.
Penalty
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