US Drug Recall Register
Class III · Low risk Terminated Initiated Feb 6, 2019 (8 years ago)

Esomeprazole Magnesium Delayed-Release Capsules USP, 40mg*, a) 90-count bottle (NDC…

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

Why it was recalled

Discoloration: Esomeprazole Magnesium DR Capsules (40mg) may contain brown pellets.

What was recalled

Esomeprazole Magnesium Delayed-Release Capsules USP, 40mg*, a) 90-count bottle (NDC 43598-510-90) b) 1000 count bottle (NDC 43598-510-10), Rx only, Mfd By: Dr. Reddy's Laboratories Limited Bachupally - 500 090 INDIA.

Recalling firm
Dr. Reddy's Laboratories, Inc.
NDC code
43598-510-90
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0995-2019

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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