Metformin Hydrochloride Tablets USP 1000 mg — Class II drug recall D-1302-2014
Terminated recall by Blu Pharmaceuticals Inc, reported 2014-05-14, distributed in CT, IL, NJ, UT. Defective container: Product distributed without inner seal on bottles.
| Recall number | D-1302-2014 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Blu Pharmaceuticals Inc, Franklin, KY, United States |
| Recall initiated | 2014-03-13 |
| Classified | 2014-05-05 |
| Reported by FDA | 2014-05-14 |
| Terminated | 2015-06-10 |
| Distributed | CT, IL, NJ, UT |
| Quantity | 101,500 tablets |
| Reason classes | packaging |
| NDC | 24658-0292-05 |
| Lot numbers | 04/15, 13E0014F1P8V |
Product
Metformin Hydrochloride Tablets USP 1000 mg, 500 tablets Rx Only, Manufactured by Blu Caribe Dorado PR 00646. Distributed by Blu Pharmaceuticals Franklin NY 42134, NDC 24658-0292-05
Reason for recall
Defective container: Product distributed without inner seal on bottles.
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-1302-2014. 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.