US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 18, 2020 (6 years ago)

Levetiracetam Tablets USP 750 mg 120-count bottles, Rx Only, Distributed by: Aurobindo…

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

Why it was recalled

CGMP Deviations: Products were manufactured in a processing area in which water leakage was observed

What was recalled

Levetiracetam Tablets USP 750 mg 120-count bottles, Rx Only, Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520, NDC 65862-247-08

Recalling firm
Aurobindo Pharma USA Inc.
NDC code
65862-247-08
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1233-2020

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 East recalls

See all