PlainRecalls
FDA Drug Moderate Class II Terminated

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

Reported: September 27, 2017 Initiated: August 30, 2017 #D-1169-2017

Product Description

Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr) Rx Only Contains: 30 Patches 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: Products no longer meet the release liner removal specification and/or z-statistic.

Details

Units Affected
321,900 patches
Distribution
Nationwide.
Location
Miami, FL

Frequently Asked Questions

What product was recalled?
Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr) Rx Only Contains: 30 Patches 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: 321,900 patches.
Why was this product recalled?
Defective Delivery System: Products no longer meet the release liner removal specification and/or z-statistic.
Which agency issued this recall?
This recall was issued by the FDA Drug on September 27, 2017. Severity: Moderate. Recall number: D-1169-2017.