US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 23, 2022 (4 years ago)

Lansoprazole Delayed-Release Capsules, USP, 30 mg, 90-count bottle, Rx Only, Manufactured…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Failed Dissolution Specifications; during long term stability testing.

What was recalled

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.

Recalling firm
Dr. Reddy's Laboratories, Inc.
NDC code
55111-399-90
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0738-2022

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 Lansoprazole recalls

See all