US Drug Recall Register
Class II · Moderate risk Terminated Initiated Dec 31, 2021 (5 years ago)

Metoprolol Tartrate Tablets, USP 25 mg, 1000 - count bottle, Rx Only, Distributed by…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Complaint received of foreign matter (metal) embedded in tablet.

What was recalled

Metoprolol Tartrate Tablets, USP 25 mg, 1000 - count bottle, Rx Only, Distributed by: TruPharma, LLC. Tampa, FL 33609; Manufactured by: Rubicon Research Prvate Limited Ambernath, Dist. Thane, 421506 India. NDC 52817-360-00

Recalling firm
Rubicon Research Private Limited
NDC code
52817-360-00
Origin
N/A, India
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0362-2022

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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