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Class II · ModerateActive recall

Metoprolol Tartrate

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

Does this affect you?
Check your lot numberLot 231037H1, exp 6/2027
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

Presence of Foreign Substance: metal in 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 byRubicon Research Private Limited, Ambernath Dist Thane 421506 India foreign manufacturer
Brand nameMETOPROLOL TARTRATE
Generic nameMETOPROLOL TARTRATE
Active ingredient(s)METOPROLOL TARTRATE
Distributed by / forTruPharma, LLC, Tampa, FL 33609
NDC52817-360-00
Show the full FDA record
Full product labelMetoprolol Tartrate Tablets USP, 25mg, 1000 count bottle, Rx only, distributed by: TruPharma, LLC, Tampa, FL 33609, Manufactured by: Rubicon Research Private Limited, Ambernath Dist Thane 421506 India, NDC 52817-360-00
Recalling firmRubicon Research Private Limited
DistributionNationwide
Quantity11,664 Bottles
Recall initiated2024-05-06
Report date2024-06-05
Recall completed—
Recall numberD-0517-2024
ClassificationClass II
FDA statusOngoing
Origin on fileAmbarnath India

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.