Noven Pharmaceuticals, Inc. Recall: Daytrana (methylphenidate transdermal system) Transder
Noven Pharmaceuticals, Inc. Recall: Daytrana (methylphenidate transdermal system) Transder is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Noven Pharmaceuticals, Inc.; Product: Daytrana (methylphenidate transdermal system) Transdermal Patch, 15 mg over 9 hours (1.6 mg/hr), packaged in
| Recalling firm | Noven Pharmaceuticals, Inc. |
|---|---|
| Product | Daytrana (methylphenidate transdermal system) Transdermal Patch, 15 mg over 9 hours (1.6 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 68968-5553-3. |
| Reason for recall | 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. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Nationwide |
| Recall initiated | 20151221 |
| Recall number | D-1438-2016 |
| Category | drug |
| State | FL |
| Country | United States |
$29/mo
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