US Drug Recall Register
Class I · High risk Terminated Initiated Aug 19, 2016 (10 years ago)

Lamotrigine Orally Disintegrating Tablets (ODT), 200 mg, 30 Tablets 3 blisters containing…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Labeling; Label Mixup; box labeled to contain 200 mg blister packs but actually contain 100 mg blister packs

What was recalled

Lamotrigine Orally Disintegrating Tablets (ODT), 200 mg, 30 Tablets 3 blisters containing 10 tablets each, Rx only, Manufactured by: Watson Pharma Private Ltd., Verna, Salcette Goa INDIA, Distributed by: Impax Generics, Hayward, CA

Recalling firm
Impax Laboratories, Inc.
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0215-2017

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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