Class II · ModerateRecall completed
Metoprolol Succinate Extended-Release Tablets
Could cause temporary or reversible harm; serious harm is unlikely.
Does this affect you?
Check your lot numberLot #: LN10686, LN10687, LN10688, LN10707, LN10708, Exp 02/15
Where it was soldNationwide
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
Failed Dissolution Specifications: failure of dissolution test observed at nine month time point.
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
Made byWockhardt Limited, Mumbai, India; Distributed by: Wockhardt USA LLC., 20 Waterview Blvd., Parsippany, NJ 07054, USA; foreign manufacturer
| Distributed by / for | Wockhardt USA LLC., 20 Waterview Blvd., Parsippany, NJ 07054, USA; |
| NDC | 64679-735-09 |
Show the full FDA record
| Full product label | Metoprolol Succinate Extended-Release Tablets, USP, 50 mg, 30-count bottle, Rx only, Manufactured by: Wockhardt Limited, Mumbai, India; Distributed by: Wockhardt USA LLC., 20 Waterview Blvd., Parsippany, NJ 07054, USA; NDC 64679-735-09, UPC 3 64679 73509 1. |
| Recalling firm | Wockhardt Usa Inc. |
| Distribution | Nationwide |
| Quantity | 109,744 bottles |
| Recall initiated | 2014-04-01 |
| Report date | 2014-05-14 |
| Recall completed | 2015-05-12 |
| Recall number | D-1300-2014 |
| Classification | Class II |
| FDA status | Terminated |
| Origin on file | Parsippany NJ United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.