US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 13, 2022 (4 years ago)

Lansoprazole Delayed-Release Orally Disintegrating Tablets, 15 mg, 100-count blisters per…

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

Why it was recalled

FAILED DISSOLUTION SPECIFICATIONS

What was recalled

Lansoprazole Delayed-Release Orally Disintegrating Tablets, 15 mg, 100-count blisters per carton, 10 Packs of 10 Tablets Each, Rx Only, Distributed by: Dr. Reddy's Laboratories, Inc., Princeton, NJ 08540, Made in India, blister barcode 4359856079, NDC 43598-560-78

Recalling firm
Dr. Reddy's Laboratories, Inc.
NDC code
43598-560-78
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1287-2022

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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