Dr. Reddy's Laboratories, Inc. recalls Lansoprazole Delayed-Release Capsules, USP, 30 mg, 90-count bottle, Rx Only, Manufactured By: Dr. Reddy's Laboratories L
Recalled April 6, 2022 · FDA recall D-0738-2022 · Dr. Reddy's Laboratories
Hazard
Failed Dissolution Specifications; during long term stability testing. · FDA Class II
Units
7,703 bottles
Sold at
Nationwide in the USA
Description
Failed Dissolution Specifications; during long term stability testing.
Product
Lansoprazole Delayed-Release Capsules, USP, 30 mg, 90-count bottle, Rx Only, Manufactured By: Dr. Reddy's Laboratories Limited, Bachupally - 500 090, India, NDC 55111-399-90.
Manufacturer(s)
Dr. Reddy's Laboratories, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →