PlainRecalls
FDA Drug Moderate Class II Terminated

Daytrana (methylphenidate transdermal system) 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: April 29, 2020 Initiated: March 31, 2020 #D-1247-2020

Product Description

Daytrana (methylphenidate transdermal system) 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
7957 30-count boxes
Distribution
Distributed Nationwide in the US
Location
Miami, FL

Frequently Asked Questions

What product was recalled?
Daytrana (methylphenidate transdermal system) 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: 7957 30-count 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 April 29, 2020. Severity: Moderate. Recall number: D-1247-2020.