Class II · ModerateActive recall
Metoprolol Succinate
Could cause temporary or reversible harm; serious harm is unlikely.
Does this affect you?
Check your lot numberLot#: a) 0686H251, 0687H251, 10688H251, Exp.: 02/2027. .
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
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 byActavis Pharma, Inc.
| Brand name | METOPROLOL SUCCINATE |
| Generic name | METOPROLOL SUCCINATE |
| Active ingredient(s) | METOPROLOL SUCCINATE |
| Distributed by / for | Teva Pharmaceuticals USA, Inc |
| NDC | 45963-678-11 |
Show the full FDA record
| Full product label | Metoprolol Succinate Extended-Release Tablets, 200 mg, 100 tablets bottles, Rx Only, Teva Pharmaceuticals, Parsippany, NJ 07054, NDC: 45963-678-11 |
| Recalling firm | Teva Pharmaceuticals USA, Inc |
| Distribution | Nationwide |
| Quantity | 19,056 bottles |
| Recall initiated | 2026-01-29 |
| Report date | 2026-03-11 |
| Recall completed | — |
| Recall number | D-0357-2026 |
| Classification | Class II |
| FDA status | Ongoing |
| 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.