Lannett Company Inc.: Drug Recall

Recall #D-0642-2025 · 08/19/2025

Class II: Risk

Recall Details

Recall Number
D-0642-2025
Classification
Class II
Product Type
Drug
Recalling Firm
Lannett Company Inc.
Status
Ongoing
Date Initiated
08/19/2025
Location
Seymour, IN, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
4,848 bottles

Reason for Recall

Presence of Foreign Tablet/Capsule: Two (2) bottles labeled as Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 10mg, 100ct, contained one (1) tablet of Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 5 mg.

Product Description

Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 10mg, 100 Tablets per bottle, Rx only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, NDC 0527-0762-37.

Distribution Pattern

OH

Other Recalls by Lannett Company Inc.

View all recalls by Lannett Company Inc. →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.