Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Daytrana (methylphenidate transdermal system) patches Recalled by Noven Therapeutics, LLC 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 Therapeutics, LLC directly.
Affected Products
Daytrana (methylphenidate transdermal system) patches, Delivers 20 mg over 9 hours (2.2 mg/hr), 30-count box, Rx only, Manufactured for Noven Therapeutics, LLC. Miami, FL 33186, NDC 68968-5554-3
Quantity: 11093 boxes
Why Was This Recalled?
Defective Delivery System: Out of specification for mechanical peel and shear.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Noven Therapeutics, LLC
Noven Therapeutics, LLC 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