Lorazepam — Class III drug recall D-580-2013
Terminated recall by Legacy Pharmaceutical Packaging LLC, reported 2013-06-12. Labeling: Incorrect or Missing Lot and/or Exp Date: Lorazepam Lot # L-04009
| Recall number | D-580-2013 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Legacy Pharmaceutical Packaging LLC, Earth City, MO, United States |
| Recall initiated | 2013-03-27 |
| Classified | 2013-06-06 |
| Reported by FDA | 2013-06-12 |
| Terminated | 2014-02-13 |
| Quantity | 1,644 bottles |
| Reason classes | labeling |
| NDC | 00904-6007-60 |
Product
Lorazepam, 0.5 mg tablets, 100 count, RX only, Distributed by Major Pharmaceuticals, Livonia, MI. NDC 0904-6007-60
Reason for recall
Labeling: Incorrect or Missing Lot and/or Exp Date: Lorazepam Lot # L-04009
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-580-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.