US Drug Recall Register
Class III · Low risk Terminated Initiated Apr 24, 2020 (6 years ago)

Esomeprazole Magnesium Delayed Release Capsules USP, 40 mg*, 1000-count bottles, Rx…

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

Why it was recalled

Discoloration: product contains brown pellets

What was recalled

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

Recalling firm
Dr. Reddy's Laboratories, Inc.
NDC code
43598-510-10
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1256-2020

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.

Other Magnesium recalls

See all