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Recall Observatory FDA recall evidence

Drug product

Daytrana (methylphenidate) transdermal system patch, Delivers 10 mg over 9 hours (1.1 mg/hr), 1 patch per pouch, packaged in 30-count patches per box, Rx only, Manufactured for Noven Therapeutics, LLC, Miami, FL 33186, By Noven Pharmaceuticals, Inc., Miami, FL 33186; NDC 68968-5552-3.

D-312-2013

January 31, 2013

Class II

Product summary

Firm
Noven Pharmaceuticals, Inc.
Event
Event 64710
Status
Terminated
Classification
Class II
Quantity
335,910 patches
Official record key
drug-enforcement:D-312-2013

Official wording

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

Code information: Lot #59824, Exp 04/13

Distribution pattern: Nationwide and Puerto Rico.

Derived failure modes

  • Potency or specification failure

    reason.potency_specification_failure · v1.0.0

    Out of Specification