Medication Administration Errors Involving Omitted Doses and Failure to Rotate Injection Sites
Summary
The facility failed to ensure residents were free from significant medication errors involving omitted doses, incorrect administration, and failure to rotate injection sites. The report identified four separate medication-related deficiencies affecting multiple residents: Trelegy was not administered to one resident as ordered, levofloxacin was not administered as ordered to another resident, heparin subcutaneous injection sites were not rotated for two residents, and insulin injection sites were not rotated for one resident. For the resident prescribed Trelegy for COPD, the physician order called for one puff daily, but the medication was documented as given on the MAR even though it was not actually administered. On observation, the nurse administered several other medications but did not give Trelegy. During interview, the nurse stated Trelegy was not available in the medication cart or facility and acknowledged the dose was missed. The DON also stated the medication had not been received from the pharmacy since the last delivery and that the resident did not have a supply after the initial 14-day quantity was used. The resident’s record showed diagnoses including glaucoma and COPD. For the resident prescribed levofloxacin for UTI, the MAR showed doses were not marked as given on two dates, and the IP confirmed the medication was not administered as ordered. The resident had diagnoses including dementia, history of falling, and UTI, and the H&P stated the resident did not have capacity to understand and make decisions. For the residents receiving heparin, the orders required subcutaneous injections with site rotation, but the LARs did not show rotation of injection sites as required. For the resident receiving insulin, the order also required rotating injection sites, but staff did not rotate the sites. The DON and RN stated that failure to rotate insulin and heparin injection sites constituted medication errors, and the facility policy and manufacturer information cited in the report required medications to be administered as ordered and injection sites to be rotated.
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