Lamivudine and Zidovudine Tablets USP 150mg/300mg 30 Unit Dose… — Class II drug recall D-1140-2015
Terminated recall by American Health Packaging, reported 2015-06-24, distributed nationwide. Failed dissolution specifications
| Recall number | D-1140-2015 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | American Health Packaging, Columbus, OH, United States |
| Recall initiated | 2015-03-02 |
| Classified | 2015-06-16 |
| Reported by FDA | 2015-06-24 |
| Terminated | 2015-10-09 |
| Distributed | Nationwide (US) |
| Reason classes | specification failure |
| NDC | 68084-0416-11, 68084-0416-21 |
| Lot numbers | 140849 |
Product
Lamivudine and Zidovudine Tablets USP 150mg/300mg 30 Unit Dose Blisters, Rx Only, Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217, Carton of 30: NDC 68084-0416-21, Individual dose: NDC 68084-0416-11
Reason for recall
Failed dissolution specifications
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-1140-2015. 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.