US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jan 20, 2021 (6 years ago)

Famotidine Tablets USP 40mg, 1,000-count bottles, Rx only, Distributed by: Aurobindo…

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

Why it was recalled

Presence of foreign tablets/capsules: Famotidine 20mg and ibuprofen 400mg tablets were found in a lot of famotidine 40mg.

What was recalled

Famotidine Tablets USP 40mg, 1,000-count bottles, Rx only, Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520 Made in India, NDC 65862-860-99

Recalling firm
Aurobindo Pharma USA Inc.
NDC code
65862-860-99
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0290-2021

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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