Metformin HCl Extended-Release Tablets — Class II drug recall D-1089-2014
Terminated recall by Caraco Pharmaceutical Laboratories, Ltd., reported 2014-03-05, distributed nationwide. Presence of Foreign Tablet; customer complaint of some tablets of Gabapentin found in a bottle of Metformin HC
| Recall number | D-1089-2014 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Caraco Pharmaceutical Laboratories, Ltd., Detroit, MI, United States |
| Recall initiated | 2014-01-28 |
| Classified | 2014-02-26 |
| Reported by FDA | 2014-03-05 |
| Terminated | 2014-09-29 |
| Distributed | Nationwide (US) |
| Quantity | 2,528 bottles |
| NDC | 62756-0142, 62756-0142-01, 62756-0142-02, 62756-0143, 62756-0143-01 |
| Lot numbers | JKM2433A |
| Expiration dates | 2016-03 |
Product
Metformin HCl Extended-Release Tablets, USP, 500 mg, Rx only, 500 count bottles, Manufactured by: Sun Pharmaceutical Inc. Ltd, Andheri (East) Mumbai-400 059, India, Distributed by: Caraco Pharmaceutical Laboratories, Ltd, Detroit, MI --- NDC 62756-142-02
Reason for recall
Presence of Foreign Tablet; customer complaint of some tablets of Gabapentin found in a bottle of Metformin HCl ER
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-1089-2014. 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.