Metoprolol Tartrate Tablets USP 50 mg — Class II drug recall D-1409-2012
Terminated recall by Teva Pharmaceuticals USA, Inc., reported 2012-07-11, distributed in OH. Tablet Thickness: Potential for some tablets not conforming to weight specifications (under and over weight)
| Recall number | D-1409-2012 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teva Pharmaceuticals USA, Inc., Sellersville, PA, United States |
| Recall initiated | 2012-05-16 |
| Classified | 2012-07-05 |
| Reported by FDA | 2012-07-11 |
| Terminated | 2013-03-22 |
| Distributed | OH |
| Quantity | 2,268 bottles |
| NDC | 00093-0733-10 |
| Lot numbers | TE1Y261 |
| Expiration dates | 2013-12 |
Product
Metoprolol Tartrate Tablets USP 50 mg, 1000 count bottle, Rx only, Manufactured in india By: Emcure Pharmaceuticals LTD. Hinjwadi, Pune, India, Manufactured for TEVA Phamaceuticals USA, Sellersville, PA 18960, NDC 0093-0733-10
Reason for recall
Tablet Thickness: Potential for some tablets not conforming to weight specifications (under and over weight)
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-1409-2012. 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.