US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Nov 6, 2019 (7 years ago)

DG Health Acid Reducer Ranitidine Tablets 150 mg, 8-count carton, Distributed by…

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

Why it was recalled

CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in Ranitidine tablets, capsules and syrups.

What was recalled

DG Health Acid Reducer Ranitidine Tablets 150 mg, 8-count carton, Distributed by: Dolgencorp LLC 100 Mission Ridge Goodletville TN 37072 NDC 55910-092-79

Recalling firm
AuroMedics Pharma LLC
NDC code
55910-092-79
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0526-2020

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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