Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Lisdexamfetamine Dimesylate Capsules Recalled by Lannett Company Inc. Due to Failed Content Uniformity Specifications: Product failed to meet...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Lannett Company Inc. directly.
Affected Products
Lisdexamfetamine Dimesylate Capsules, 10 mg, 100 Capsules per bottle, Rx only, Distributed by: Lannet Company, Philadelphia, PA 19136, NDC: 0527-4661-37
Quantity: 1608 bottles
Why Was This Recalled?
Failed Content Uniformity Specifications: Product failed to meet the action limits for stratified content uniformity.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Lannett Company Inc.
Lannett Company Inc. has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report