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

Lansoprazole Delayed-Release Capsules, USP, 15 mg, a) 30-count bottle, (NDC…

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, 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

Recalling firm
Dr. Reddy's Laboratories, Inc.
NDC code
55111-398-30
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0737-2022

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.

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