Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours Recalled by Noven Pharmaceuticals Inc Due to Defective Delivery System: Customer complaints received for ripping...

Date: June 24, 2022
Company: Noven Pharmaceuticals Inc
Status: Ongoing
Source: FDA (Drug)

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 10 mg over 9 hours (1.1 mg/hr) Contains: 30 Patches, Rx only, Manufactured for Noven Therapeutics, LLC, Miami, FL 33186 By Noven Pharmaceuticals, Inc., Miami, FL 33186. NDC 68968-5552-3

Quantity: 8,559 cartons

Why Was This Recalled?

Defective Delivery System: Customer complaints received for ripping patches and tight release/adhesive transfer.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Noven Pharmaceuticals Inc

Noven Pharmaceuticals Inc has 18 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report