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Lannett Company Inc.

Lannett Company Inc. Recalls

All product recalls associated with Lannett Company Inc..

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Recall Summary

Total Recalls

Past Year

Class I (Serious)

Most Recent

Oct 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–3 of 3 recalls

Niacin Extended-release Tablets (Lannett) – dissolution failure (2025)

Failed Dissolution Specifications

Class IIModerate

FDAOct 10, 2025Nationwide• Lannett Company Inc.

Dextroamphetamine Tablets (Lannett Company) - Foreign Tablet (2025)

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.

Class IIModerate

FDAAug 19, 2025OH• Lannett Company Inc.

Lisdexamfetamine Capsules (Lannett) - Label Mix-up (2025)

Labeling: Label Mix-up. A bottle labeled as Lisdexamphetamine Dimesylate Capsules 40mg, contained Lisdexamphetamine Dimesylate Capsules 30mg.

Class IIModerate

FDAAug 11, 2025Nationwide• Lannett Company Inc.