Medication administration, emergency kit, and controlled substance record failures
Summary
The facility failed to notify Resident 262’s physician when Spironolactone, an active order for CHF, was unavailable on 02/16/2026. Resident 262 had diagnoses including hypertensive heart disease, and the record also showed the resident’s cognitive skills were intact on the MDS, while the H&P stated the resident did not have the capacity to make healthcare decisions. The MAR for 02/16/2026 showed the scheduled 9:00 AM dose was marked with code 4, and nursing documentation indicated the medication was not available. LVN 3 stated she did not notify the pharmacy on 02/16/2026, did not notify the prescriber, and did not document that the resident missed the dose. The DON reviewed the MAR and progress notes and stated there was no documentation explaining why the medication was held and no documentation that the physician was notified. The facility also failed to positively identify residents before administering medications. During a medication pass, LVN 3 administered Apixaban, Escitalopram, and Benztropine to Resident 262 after stating the resident’s name, but she was not observed verifying identity before administration. LVN 3 stated she already knew the resident and that she asked the resident’s name, but the resident could not hear her and was complaining of hearing difficulty. During another medication pass, LVN 6 administered seven medications to Resident 260, including Labetalol, Lisinopril, Vitamin C, Cranberry, Vitamin B12, Magnesium Oxide, and Ferrous Gluconate, without being observed checking the resident’s identification band. LVN 6 later stated she should have checked the resident’s identification band and that nurses were supposed to verify resident identification before giving medications. The facility did not maintain accurate Ekit usage records for all residents. During inspection, RN 1 stated the facility did not keep a copy of the Ekit usage log; instead, the log was faxed to the pharmacy and then placed back inside the Ekit and sent with the kit to the pharmacy. RN 1 stated this applied to controlled Ekits, injectable Ekits, and non-controlled Ekits. The DON stated the facility did not have a process to monitor or track Ekit usage. The facility also failed to ensure controlled drugs were counted and signed for together during shift change. One controlled drugs inventory form had blank incoming and outgoing signatures for a shift change, and an LVN stated both nurses counted the controlled medications but forgot to sign. Another LVN stated she signed the form ahead of time before the next nurse arrived. The ADON stated both incoming and outgoing nurses were required to count and sign together, and that failing to do so could result in uncertainty about the accuracy of the controlled medications.
Penalty
Resources
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