US Drug Recall Register
Class II · Moderate risk Terminated Initiated Oct 5, 2021 (5 years ago)

Omeprazole Delayed-Release Capsules, 20 mg* (equivalent to 20.6 mg omeprazole magnesium)…

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

Why it was recalled

CGMP Deviations: Customer complaint for the presence of a staple co-mingled with capsules within the bottle.

What was recalled

Omeprazole Delayed-Release Capsules, 20 mg* (equivalent to 20.6 mg omeprazole magnesium), 24 Hour, 14-count capsules per bottle within a carton, Distributed by Cardinal Health, Dublin, OH 43017, NDC 70000-0232-1

Recalling firm
Dr. Reddy's Laboratories, Inc.
NDC code
70000-0232-1
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0026-2022

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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