Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Daytrana (methylphenidate transdermal system) CII Recalled by Noven Pharmaceuticals Inc Due to Defective Delivery System: Out of specification for shear.
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) CII, 10mg, 30-count carton, Rx only, Manufactured for Noven Therapeutics, LLC., Miami by Noven Pharmaceuticals, Inc., NDC 68968-5552-3.
Quantity: N/A
Why Was This Recalled?
Defective Delivery System: Out of specification for shear.
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