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Apotex Inc. recalls Rite Aid Pharmacy Maximum Strength Ranitidine Tablets, USP 150 mg-acid reducer Distributed By: Rite Aid 30 Hunter Lane C

Recalled November 20, 2019 · FDA recall D-0319-2020 · Apotex

Hazard
GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine (NDMA). · FDA Class II
Units
215,387 bottles
Sold at
Nationwide

Description

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

Product
Rite Aid Pharmacy Maximum Strength Ranitidine Tablets, USP 150 mg-acid reducer Distributed By: Rite Aid 30 Hunter Lane Camp Hill, PA 17011 a) 50 tablets NDC 11822-6052-1; b) 65 tablets NDC 11822-6052-2; c) 95 tablets NDC 11822-4727-3; d) 24 tablets NDC 11822-6051-8
Manufacturer(s)
Apotex Inc.
Made in
Canada

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Apotex Inc. recalls Rite Aid Pharmacy Maximum Strength Ranitidine Tablets, USP 150 mg-acid reducer Distributed By: Rite Aid 30 Hunter Lane C | RecallWatchUSA