RecallRadar

FDA Drug recall D-0833-2020

Lamotrigine Tablets, USP, 100 mg, Rx Only, 100-count bottle, Mfd. by: Taro Pharmaceutical Industries Ltd

On 2020-02-19 the FDA classified a Class I recall of Lamotrigine Tablets, USP, 100 mg, Rx Only, 100-count bottle, Mfd. by: Taro Pharmaceutical Industries Ltd by Taro Pharmaceuticals U, citing cross Contamination; Lamotrigine Tablets 100 mg USP was contaminated with enalapril maleate.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0833-2020
ClassificationClass I
Statusterminated
Initiated2019-12-20
Published2020-02-19
Last updated2026-09-13 11:52 UTC
CompanyTaro Pharmaceuticals U
DistributionUS

Product

Lamotrigine Tablets, USP, 100 mg, Rx Only, 100-count bottle, Mfd. by: Taro Pharmaceutical Industries Ltd. Haifa Bay, Israel 2624761 Dist. by: Taro Pharmaceuticals U.S.A., Inc. Hawthorne, NY 10532, NDC 51672-4131-1.

Reason

Cross Contamination; Lamotrigine Tablets 100 mg USP was contaminated with enalapril maleate.

Identifiers

ndc51672-4130-6
ndc51672-4130-4
ndc51672-4130-1
ndc51672-4130-3
ndc51672-4130-0
ndc51672-4131-6
ndc51672-4131-4
ndc51672-4131-1
ndc51672-4131-3
ndc51672-4131-0
ndc51672-4132-6
ndc51672-4132-4
ndc51672-4132-1
ndc51672-4132-2
ndc51672-4132-3
ndc51672-4132-0
ndc51672-4133-6
ndc51672-4133-4
ndc51672-4133-1
ndc51672-4133-2
ndc51672-4133-3
ndc51672-4133-0
code_infoLot #: 331771, Exp. June 2021

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0833-2020%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.