US Drug Recall Register
Class II · Moderate risk Completed Initiated Sep 24, 2019 (7 years ago)

Walgreens Maximum Strength Wal-Zan 150 Ranitidine Tablets, USP 150 mg/Acid Reducer…

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

Why it was recalled

GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine (NDMA).

What was recalled

Walgreens Maximum Strength Wal-Zan 150 Ranitidine Tablets, USP 150 mg/Acid Reducer Distributed By: Walgreen Co., 200 Wilmot RD., Deerfield, IL 60015 a) 200 Tablets NDC 0363-1030-07; b) 24 Tablets NDC 0363-1030-02; c) 95 Tablets NDC 0363-1030-09; d) 65 Tablets NDC 0363-1030-06

Recalling firm
Apotex Inc.
NDC code
0363-1030-07
Origin
N/A, Canada
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0314-2020

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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