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Recall Observatory FDA recall evidence

Drug product

Daytrana (methylphenidate transdermal system) Transdermal Patch, 20 mg over 9 hours (2.2 mg/hr), packaged in 30-count patches per box, Rx only, Manufactured by Noven Therapeutics, LLC, Miami, FL 33186; By Noven Pharmaceuticals, Inc., Miami, FL 33186, NDC 68968-5554-3.

D-1439-2016

December 21, 2015

Class II

Product summary

Firm
Noven Pharmaceuticals, Inc.
Event
Event 73718
Status
Terminated
Classification
Class II
Quantity
2088 boxes
Official record key
drug-enforcement:D-1439-2016

Official wording

Reason: Defective Delivery System: Out of Specification (OOS) results for the mechanical peel force (MPF) and z-statistic value which relates to the patients and caregiver ability to remove the release liner from the patch adhesive prior to administration.

Code information: Lot # 77140, Exp 05/16

Distribution pattern: Nationwide

Derived failure modes

  • Potency or specification failure

    reason.potency_specification_failure · v1.0.0

    Out of Specification