US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Mar 1, 2019 (8 years ago)

Losartan Potassium Tablets, USP, 50 mg, 30 tablet bottles, Rx Only, Distributed by…

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

Why it was recalled

CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA) detected

What was recalled

Losartan Potassium Tablets, USP, 50 mg, 30 tablet bottles, Rx Only, Distributed by: Wal-Mart, Bentonville, AR 72716, Manufactured for: Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, Packaged by: Legacy Pharmaceutical Packaging LLC, Earth City, MO 63045. NDC 68645-578-54

Recalling firm
Legacy Pharmaceutical Packaging LLC
NDC code
68645-578-54
Origin
MO, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1049-2019

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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