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: Recalled lot was found to...
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), 30 patches per box, Rx only, Manufactured for Noven Therapeutics, LLC, Miami, FL 33186; By Noven Pharmaceuticals, Inc., Miami, FL 33186, NDC 68968-5553-3.
Quantity: 3977 boxes
Why Was This Recalled?
Defective Delivery System: Recalled lot was found to be out of specification for shear. Shear is an attribute related to the adhesive properties of the transdermal patches.
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