Metoprolol Succinate Extended-Release Tablets — Class II drug recall D-0727-2018
Terminated recall by Dr. Reddy's Laboratories, Inc., reported 2018-05-16, distributed nationwide. Presence of Foreign Tablets/Capsules: One foreign tablet identified as Clopidogrel 75 mg was found in a 100 co
| Recall number | D-0727-2018 |
|---|---|
| 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 | 2018-04-23 |
| Classified | 2018-05-09 |
| Reported by FDA | 2018-05-16 |
| Terminated | 2020-12-14 |
| Distributed | Nationwide (US) |
| Quantity | 8,160 bottles |
| NDC | 55111-0468, 55111-0468-01, 55111-0468-05, 55111-0468-30, 55111-0468-60, 55111-0468-78, 55111-0468-79, 55111-0469, 55111-0469-01, 55111-0469-05, 55111-0469-30, 55111-0469-60, 55111-0469-78, 55111-0469-79 |
| Lot numbers | C706254 |
Product
Metoprolol Succinate Extended-Release Tablets, USP, 100 mg, 100 Tablets bottle, Rx only, Manufactured by: Dr. Reddy's Laboratories Limited Bachupally-500 090 India\ NDC 55111-468-01
Reason for recall
Presence of Foreign Tablets/Capsules: One foreign tablet identified as Clopidogrel 75 mg was found in a 100 count bottle of Metoprolol Succiante Extended-Release Tablets.
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-0727-2018. 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.