PlainRecalls
FDA Drug Moderate Class II Ongoing

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

Reported: July 6, 2022 Initiated: June 24, 2022 #D-1169-2022

Product Description

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

Reason for Recall

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

Details

Recalling Firm
Noven Pharmaceuticals Inc
Units Affected
8,559 cartons
Distribution
Distributed Nationwide in the USA
Location
Miami, FL

Frequently Asked Questions

What product was recalled?
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. Recalled by Noven Pharmaceuticals Inc. Units affected: 8,559 cartons.
Why was this product recalled?
Defective Delivery System: Customer complaints received for ripping patches and tight release/adhesive transfer.
Which agency issued this recall?
This recall was issued by the FDA Drug on July 6, 2022. Severity: Moderate. Recall number: D-1169-2022.