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Recall Observatory FDA recall evidence

Drug product

Daytrana (methylphenidate) transdermal system patch, Delivers 30 mg over 9 hours (3.3 mg/hr), 1 patch per pouch (NDC 54092-555-01), packaged in 30-count patches per box (NDC 54092-555-30), Rx only, Manufactured for Shire US Inc., Wayne, PA 19087 by Noven Pharmaceuticals, Inc., Miami, FL 33186.

D-1373-2012

July 05, 2011

Class II

Product summary

Firm
Noven Pharmaceuticals, Inc.
Event
Event 61891
Status
Terminated
Classification
Class II
Quantity
242,100 patches
Official record key
drug-enforcement:D-1373-2012

Official wording

Reason: Miscalibrated and/or Defective Delivery System: Out of Specification results for mechanical peel force and/or the z-statistic value which relates to the patient's ability to remove the release liner from the patch adhesive prior to administration.

Code information: Lot #: 43008, Exp 01/12; 48591, Exp 10/12

Distribution pattern: Nationwide and Puerto Rico.

Derived failure modes

  • Potency or specification failure

    reason.potency_specification_failure · v1.0.0

    Out of Specification