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 Labeling: Label Mix-up. A bottle labeled as Lisdexamphetamine...
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, 40 mg, 100-count bottles, Rx Only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136. NDC 0527-4664-37
Quantity: 8544 bottles
Why Was This Recalled?
Labeling: Label Mix-up. A bottle labeled as Lisdexamphetamine Dimesylate Capsules 40mg, contained Lisdexamphetamine Dimesylate Capsules 30mg.
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