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Class II · ModerateRecall completed

Metoprolol Tartrate

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

Does this affect you?
Check your lot numberLot: MJ1019025-A, Exp. date 04/2022
Where it was soldNationwide within the United States
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

Presence of Foreign Substance: Product complaints received for the presence of metal wire in one tablet.

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 byAurobindo Pharma Limited
Brand nameMETOPROLOL TARTRATE
Generic nameMETOPROLOL TARTRATE
Active ingredient(s)METOPROLOL TARTRATE
Distributed by / forAurobindo Pharma USA Inc. 279 Princeton-Highstown Road East Windsor, NJ 08520
NDC65862-064-99
Show the full FDA record
Full product labelMetoprolol Tartrate Tablets USP 100 mg, 1000-count bottles, Rx only, Distributed by: Aurobindo Pharma USA Inc. 279 Princeton-Highstown Road East Windsor, NJ 08520, NDC 65862-064-99
Recalling firmAurobindo Pharma USA Inc.
DistributionNationwide within the United States
Quantity2,820 bottles
Recall initiated2021-09-09
Report date2021-09-29
Recall completed2023-10-31
Recall numberD-0812-2021
ClassificationClass II
FDA statusTerminated
Origin on fileEast Windsor 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.