Medication Labeling, Storage, and Disposal Deficiencies
Summary
Surveyors identified a deficiency in the facility’s pharmacy services related to medication labeling, storage, and disposal. Facility policy required prescription medications to be labeled with the resident’s name and other key information, and nonprescription medications to remain in the manufacturer’s container and identified with the resident’s name. During inspection of a medication cart, surveyors found 22 packets of 5% lidocaine patches rubber-banded together with no pharmacy label or resident identification. The LVN assigned to the cart stated that two residents had orders for lidocaine patches and that someone must have removed the packets from the manufacturer’s box, confirming there was no label to indicate which residents the packets belonged to. The DON and the consultant pharmacist both confirmed that non–over-the-counter medications should have resident labels and that the labeled box and packets should not have been separated. The facility also failed to ensure expired and beyond-use-date medications were separated and removed from active stock as required by its policy on discontinued medications. In one medication room, surveyors observed a manufacturer box of ferrous gluconate 325 mg unit-dose tablets on the shelf with a manufacturer expiration date that had already passed; the RN present verified the medication was expired and should not have been on the shelf. On multiple medication carts, surveyors found expired blister packs of cyclobenzaprine and clonidine with past expiration dates still stored with active medications; the LVNs confirmed these medications were expired and should have been removed for destruction. Additionally, two Lantus Solostar insulin pens on a cart were found with open dates indicating they had been in use longer than the 28 days specified on the pharmacy label and manufacturer information, and the LVN confirmed both pens were expired but still present on the cart. Further deficiencies were identified in the labeling and handling of multi-dose injectable vials and insulin pens. Facility policy required multi-dose vials to be labeled with the date opened and initials of the first user. In a medication room refrigerator, surveyors observed a multi-dose vial of cyanocobalamin with the protective cap removed, visibly used, but without an open date; the RN confirmed an open date should have been on the vial. On a medication cart, a Novolog insulin pen stored at room temperature had no open date, and on another cart, Lantus and Humalog insulin pens also lacked open dates on the pens or pharmacy labels; the LVNs acknowledged that staff needed to enter the open dates. The consultant pharmacist stated that the time period for insulin pen use begins when the pens are removed from the refrigerator, underscoring that open dating was required but not done. Surveyors also found that medications were not properly stored at the bedside for two residents. One resident, who was cognitively able to follow commands and answer appropriately per a prior H&P, had a container of antacid tablets from home on the overbed table, with about one-third of the tablets remaining. When asked, the resident stated she took them when needed and did not want to bother staff. Review of the MAR showed PRN orders for calcium carbonate and simethicone, but these medications were not documented as administered. An LVN and an RN both acknowledged that the antacid container should not have been on the overbed table, and the resident became upset when the LVN attempted to remove it. In another case, a resident who was documented as unable to make decisions had a three-quarters full bottle of povidone-iodine on the overbed table while a family member was present. The resident had physician orders for povidone-iodine treatment to bilateral heel DTIs. Nursing staff confirmed the bottle’s presence on the overbed table and stated that no medications should be at bedside, noting that family sometimes placed items there.
Penalty
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