Recalls / Active ingredient / Levetiracetam

Levetiracetam

9 FDA drug recalls involving the active ingredient “Levetiracetam” — 2 Class I.

Date	Class	Product	Firm
2025-03-13	Class I	Levetiracetam 0.75% in Sodium Chloride Injection 1,000 mg/100 mL (10 mg/mL), 1 x 100mL, Rx Only, Manufactured	Dr. Reddy's Laboratories, Inc.
2020-03-18	Class II	Levetiracetam Tablets USP 750 mg 120-count bottles, Rx Only, Distributed by: Aurobindo Pharma USA, Inc. 279	Aurobindo Pharma USA Inc.
2019-07-18	Class II	Keppra (levetiracetam) 1000 mg tablets, 60 tablets per bottle, Rx only, Manufactured for UCB, Inc. Smyrna, GA	Ucb, Inc
2018-10-26	Class I	Levetiracetam in 0.54 % Sodium Chloride Injection 1,500/mg/100mL (15mg/mL), For intravenous Infusion Only, 1 x	Dr. Reddy's Laboratories, Inc.
2018-03-27	Class II	Levetiracetam in 0.54% Sodium Chloride Injection, 1,500 mg per 100 mL (15 mg/mL), For Intravenous Infusion Onl	AuroMedics Pharma LLC
2018-03-27	Class II	Levetiracetam in 0.82% Sodium Chloride Injection, 500 mg per 100 mL (5 mg/mL), For Intravenous Infusion Only,	AuroMedics Pharma LLC
2018-03-27	Class II	Levetiracetam in 0.75% Sodium Chloride Injection, 1000 mg per 100 mL (10 mg/mL), For Intravenous Infusion Only	AuroMedics Pharma LLC
2017-10-12	Class II	Levetiracetam Oral Solution, USP, 100 mg/mL, packaged in a 16 fl oz (473 mL) bottle, Rx only, Manufactured for	Hetero Labs, Ltd. - Unit III
2012-07-27	Class II	Levetiracetam Tablets, USP 500 mg, 500 count bottle, Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Mor	Mylan Pharmaceuticals Inc.