US Drug Recall Register
Class II · Moderate risk Terminated Initiated May 29, 2015 (11 years ago)

Losartan potassium tablets USP, 50 mg, 90-count bottle, Rx only, Manufactured for Apotex…

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

Why it was recalled

Failed Content Uniformity Specifications: The product may not meet the limit for blend uniformity specification.

What was recalled

Losartan potassium tablets USP, 50 mg, 90-count bottle, Rx only, Manufactured for Apotex Inc 150 Signet Drive, ON M9L1T9 by Apotex Research Private Limited, Plot 1 & 2, Bommasandra Industrial Area, 4th Phase Jigani Link Road, Bangalore, Karnataka, 560099, India NDC 60505-3161-9

Recalling firm
Apotex Inc.
NDC code
60505-3161-9
Origin
N/A, Canada
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1214-2015

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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