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Class II · ModerateActive recall

Metoprolol Succinate

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot # 25140859; Exp. Date: Jan 2027
Where it was soldU.S. Nationwide
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

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byAlkem Laboratories Ltd., India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054 foreign manufacturer
Brand nameMETOPROLOL SUCCINATE
Generic nameMETOPROLOL SUCCINATE ER TABLETS
Active ingredient(s)METOPROLOL SUCCINATE
Distributed by / forAscend Laboratories, LLC, Parsippany, NJ 07054
NDC67877-590-01
Show the full FDA record
Full product labelAscend Laboratories, LLC, Metoprolol Succinate Extended-Release Tablets, USP, 25 mg* Rx Only, Manufactured by: Alkem Laboratories Ltd., India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054, NDC 67877-590-01.
Recalling firmAscend Laboratories, LLC
DistributionU.S. Nationwide
Quantity17,304 100-count bottles
Recall initiated2026-04-27
Report date2026-05-20
Recall completed—
Recall numberD-0547-2026
ClassificationClass II
FDA statusOngoing
Origin on fileBedminster NJ United States

Related

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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.