AVKARE Inc. recalls Lamotrigine Tablets, USP, 150 mg, Rx Only, a) 60 count Bottle, NDC 42291-368-60, b) 500 count Bottle, NDC 42291-368-50,
Recalled June 10, 2020 · FDA recall D-1289-2020 · AVKARE
Hazard
Presence of Foreign Substance consistent with granules from desiccant packs used during storage · FDA Class III
Units
4124 bottles
Sold at
Nationwide in the U.S.
Description
Presence of Foreign Substance consistent with granules from desiccant packs used during storage
Product
Lamotrigine Tablets, USP, 150 mg, Rx Only, a) 60 count Bottle, NDC 42291-368-60, b) 500 count Bottle, NDC 42291-368-50, Manufactured for: AvKARE, Inc. Pulaski, TN 38478.
Manufacturer(s)
AVKARE Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →