Lamotrigine: 5 recalls on record

Recalled by 1 agency: FDA (5).

First recall on record: October 5, 2016. Most recent: August 17, 2022.

Risk classification: Class I: 1 · Class II: 1 · Class III: 3

Most recent recalls

DateAgencyProduct
August 17, 2022FDALamotrigine Tablets, USP 100 mg, 1000-count bottles, Rx Only, Manufactured for: AvKARE, I…D-1329-2022
June 10, 2020FDALamotrigine Tablets, USP, 150 mg, Rx Only, a) 60 count Bottle, NDC 42291-368-60, b) 500 c…D-1289-2020
February 19, 2020FDALamotrigine Tablets, USP, 100 mg, Rx Only, 100-count bottle, Mfd. by: Taro Pharmaceutica…D-0833-2020
September 26, 2018FDALamotrigine Extended-Release Tablets, USP, 200 mg, 30 tablets per bottle, Rx Only, Manufa…D-1204-2018
October 5, 2016FDALamotrigine Tablets, USP, 150 mg, 500-count Tablets per bottle, Rx only, Manufactured by…D-1519-2016

Questions about this brand

How many recalls does Lamotrigine have?
Recalert has 5 U.S. recalls on record for Lamotrigine, published between October 5, 2016 and August 17, 2022.
What was the most recent Lamotrigine recall?
FDA recall D-1329-2022, published August 17, 2022: Lamotrigine Tablets, USP 100 mg, 1000-count bottles, Rx Only, Manufactured for: AvKARE, Inc. Pulaski, TN 38478, NDC 42291-367-10, UPC 3 42291 36710 4
Which agencies have recalled Lamotrigine products?
Lamotrigine products appear in recalls from: FDA (5).

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