FDA Drug Recalls

Recalls / Firms / Lannett Company Inc.

Lannett Company Inc.

12 FDA drug recalls on record1 Class I.

DateClassDrugStatus
2025-10-10Class IINiacinOngoing
2025-08-19Class IIDextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate And Amphetamine SulfateOngoing
2025-08-11Class IILisdexamfetamine DimesylateCompleted
2024-10-25Class IILisdexamfetamine DimesylateTerminated
2022-11-09Class IIITriamterene and Hydrochlorothiazide Capsules, USP (37.5 mg/25 mg), Rx Only, 1000 Capsules Terminated
2022-11-09Class IIITriamterene and Hydrochlorothiazide Capsules, USP (37.5 mg/25 mg), Rx Only, [100 or 1000 ]Terminated
2022-02-09Class IIDiazepam Oral Solution (Concentrate), 25 mg per 5 mL (5 mg/mL), 30 mL BOTTLE and DROPPER, Terminated
2020-08-10Class IIPrednisone Tablets, USP 2.5 mg, 100 tablets, Rx only, Distributed by: Lannett Company, InTerminated
2019-12-06Class ILevetiracetam Oral Solution 100mg/mL, 473 mL (16 fl. oz.) Bottles, Rx Only, Distributed byTerminated
2019-10-28Class IILannett Ranitidine Syrup (Ranitidine Oral Solution, USP), 15mg/mL Rx Only Distributed by:Terminated
2019-02-21Class IIIOxybutynin ChlorideTerminated
2018-10-11Class IIHydroxyzine HydrochlorideTerminated