Dr — Class II drug recall D-1080-2014
Terminated recall by Dr. Reddy's Laboratories, Inc., reported 2014-02-12, distributed in LA, MI, MO, MS, OH. Failed Dissolution Specification; 12-Month stability interval.
| Recall number | D-1080-2014 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Dr. Reddy's Laboratories, Inc., Princeton, NJ, United States |
| Recall initiated | 2013-12-13 |
| Classified | 2014-02-06 |
| Reported by FDA | 2014-02-12 |
| Terminated | 2015-02-12 |
| Distributed | LA, MI, MO, MS, OH |
| Quantity | 8,592 bottles |
| Reason classes | specification failure |
| NDC | 55111-0466, 55111-0466-01, 55111-0466-05, 55111-0466-30, 55111-0466-60, 55111-0466-78, 55111-0466-79, 55111-0467, 55111-0467-01, 55111-0467-05, 55111-0467-30, 55111-0467-60, 55111-0467-78, 55111-0467-79 |
| Lot numbers | C207416, C207420 |
Product
Dr. Reddy's Metoprolol Succinate Extended-Release Tablets USP, 50 mg 100 tablets Rx Only Mfd. By: Dr. Reddy's Laboratories Limited Bachepalli -500 090 INDIA NDC 55111-467-01
Reason for recall
Failed Dissolution Specification; 12-Month stability interval.
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-1080-2014. 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.