US Drug Recall Register
Class III · Low risk Terminated Initiated Jun 21, 2022 (4 years ago)

Esomeprazole Magnesium Delayed-Release Capsules, USP, 40mg, Rx Only, 90 Capsules per…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Superpotent Drug: Out of specification for assay at the 12-month timepoint.

What was recalled

Esomeprazole Magnesium Delayed-Release Capsules, USP, 40mg, Rx Only, 90 Capsules per bottle, Manufactured by: Ohm Laboratories Inc. New Brunswick, NJ 08901, Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, NDC 63304-735-90.

Recalling firm
Sun Pharmaceutical Industries INC
NDC code
63304-735-90
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0005-2023

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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