Deficient Medication Storage and Labeling Practices
Summary
Surveyors identified multiple deficiencies in the facility's medication storage and labeling practices. In two of three medication carts, medications were not stored according to the facility's policy and professional standards. Specifically, a vial of atropine sulfate ophthalmic solution intended for sublingual use was stored in the same bin as acetaminophen rectal suppositories, contrary to the policy requiring separation of oral, ophthalmic, and rectal medications. Additionally, an unopened bottle of latanoprost ophthalmic solution was found without an open date label and was not stored in the refrigerator as required by the manufacturer's instructions. Staff interviews confirmed that these storage practices were not in line with facility policy or manufacturer requirements, and that proper labeling was necessary to ensure medication safety and efficacy. Further deficiencies were observed in the medication room refrigerators. In one refrigerator, several medications, including insulin, Tubersol, acetylcysteine, and Dupixent, were stored at 35°F, which is below the manufacturer-recommended range of 36°F to 46°F. The refrigerator also had a buildup of ice, which is not appropriate for medication storage. Staff acknowledged that these conditions could compromise the integrity of the medications. In another medication room refrigerator, a bottle of prednisolone acetate ophthalmic suspension was stored in the refrigerator, despite manufacturer instructions to store it at room temperature and protect it from freezing. Staff confirmed that this was not the correct storage method and could affect the medication's effectiveness. The facility's policy and procedure on medication storage requires that medications and biologicals be stored according to manufacturer recommendations and that internally administered medications be kept separate from externally used medications. Staff interviews consistently indicated awareness of these requirements, but observations revealed that these standards were not consistently followed. The deficiencies involved multiple residents and had the potential to affect the safety and effectiveness of their prescribed medications.
Penalty
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