Dr. Reddy's Laboratories, Inc. recalls Lansoprazole Delayed-Release Capsules, USP, 15 mg, a) 30-count bottle, (NDC 55111-398-30), b) 90-count bottle, (55111-39
Recalled April 6, 2022 · FDA recall D-0737-2022 · Dr. Reddy's Laboratories
Hazard
Failed Dissolution Specifications; during long term stability testing. · FDA Class II
Units
8,352 bottles (30-count), 1,368 bottles (90-count)
Sold at
Nationwide in the USA
Description
Failed Dissolution Specifications; during long term stability testing.
Product
Lansoprazole Delayed-Release Capsules, USP, 15 mg, a) 30-count bottle, (NDC 55111-398-30), b) 90-count bottle, (55111-398-90), Rx Only, Manufactured. By: Dr. Reddy's Laboratories Limited, Bachupally - 500 090, India
Manufacturer(s)
Dr. Reddy's Laboratories, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →