PlainRecalls
FDA Drug Moderate Class II Terminated

Daytrana (methylphenidate transdermal system) patches, Delivers 10 mg over 9 hours (1.1 mg/hr), 30-count box, Rx only, Manufactured for Noven Therapeutics, LLC. Miami, FL 33186, NDC 68968-5552-3

Reported: March 25, 2020 Initiated: March 2, 2020 #D-1042-2020

Product Description

Daytrana (methylphenidate transdermal system) patches, Delivers 10 mg over 9 hours (1.1 mg/hr), 30-count box, Rx only, Manufactured for Noven Therapeutics, LLC. Miami, FL 33186, NDC 68968-5552-3

Reason for Recall

Defective Delivery System: Out of specification for mechanical peel and shear.

Details

Recalling Firm
Noven Therapeutics, LLC
Units Affected
9513 boxes
Distribution
U.S.A. Nationwide
Location
Miami, FL

Frequently Asked Questions

What product was recalled?
Daytrana (methylphenidate transdermal system) patches, Delivers 10 mg over 9 hours (1.1 mg/hr), 30-count box, Rx only, Manufactured for Noven Therapeutics, LLC. Miami, FL 33186, NDC 68968-5552-3. Recalled by Noven Therapeutics, LLC. Units affected: 9513 boxes.
Why was this product recalled?
Defective Delivery System: Out of specification for mechanical peel and shear.
Which agency issued this recall?
This recall was issued by the FDA Drug on March 25, 2020. Severity: Moderate. Recall number: D-1042-2020.