Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Daytrana (methylphenidate transdermal system) Recalled by Noven Pharmaceuticals Inc Due to Defective Delivery System: Out of specification for mechanical...
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 Noven Pharmaceuticals Inc directly.
Affected Products
Daytrana (methylphenidate transdermal system), Delivers 15 mg over 9 hours (1.6 mg/hr), Contains: 30 Patches in in a foil-sealed polypropylene tray, packed in a paper carton, Rx only, Manufactured for Noven Therapeutics, LLC, Miami, FL, 33186, By Noven Pharmaceuticals, Inc., Miami, FL, 33186, NDC 68968-5553-3.
Quantity: 551,670 patches
Why Was This Recalled?
Defective Delivery System: Out of specification for mechanical peel.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Noven Pharmaceuticals Inc
Noven Pharmaceuticals Inc has 18 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report