Lannett Company Inc. recalls
6 federal recalls on file, showing the 3 from the last 12 months. We monitor every CPSC, FDA, USDA, and NHTSA notice for Lannett Company Inc. and translate it into plain English — free weekly digest, optional same-day alerts.
- 2026-07-08FDA-DrugClass IILannett amphetamine capsules recalled for labeling mix-up
Lannett Company distributed amphetamine extended-release capsules that contained only immediate-release pellets but were labeled as extended-release. This labeling error could result in incorrect dosing and medication timing for patients who depend on the extended-release formulation.
- 2026-05-27FDA-DrugClass IIILannett Primidone tablets recalled for API contamination
Lannett Company's Primidone Tablets 250mg were contaminated during manufacturing with trace amounts of Acemetacin, a different active pharmaceutical ingredient. The contamination affected specific lot numbers distributed nationwide. No injuries have been reported.
- 2025-10-29FDA-DrugClass IINiacin Extended-release Tablets, USP, 1,000 mg, Rx Only, 90 Tablets per bottle, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136. NDC: 62175-322-46
Failed Dissolution Specifications
Get the week's recalls, including Lannett Company Inc.
Free weekly digest — every federal recall affecting your household, Lannett Company Inc. included when it comes up. Track Lannett Company Inc. specifically with Always-on.