Dr — Class II drug recall D-1381-2014
Terminated recall by Dr. Reddy's Laboratories, Inc., reported 2014-06-18, distributed nationwide. Failed Dissolution Specifications: Failure of dissolution test observed at the 18 month time point.
| Recall number | D-1381-2014 |
|---|---|
| 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 | 2014-05-23 |
| Classified | 2014-06-12 |
| Reported by FDA | 2014-06-18 |
| Terminated | 2015-05-01 |
| Distributed | Nationwide (US) |
| Quantity | 13,560 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 | C206578, C207415 |
| Expiration dates | 2014-05, 2014-06 |
Product
Dr. Reddy's Metoprolol Succinate Extended Release Tablets, USP 25 mg. 100-count bottle, Rx only, Manufactured By: Dr. Reddy's Laboratories Limited, Batchupally - 500 090 India. NDC55111-466-01
Reason for recall
Failed Dissolution Specifications: Failure of dissolution test observed at the 18 month time point.
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-1381-2014. 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.