Every recall we track for Noven Therapeutics, LLC — 7 in all, all from 2020 — plus the complaints and injury reports the public filed about them.
Noven Therapeutics recalls Daytrana (methylphenidate transdermal system) 30-count boxes due to defective delivery system causing inconsistent dosing. No remedy specified in official notice.
Noven Therapeutics recalls Daytrana (methylphenidate transdermal patches) due to defective delivery system causing incorrect dosing. 30-count boxes with specific NDC numbers are affected.
7 recalls from Noven Therapeutics, LLC are on record with U.S. safety agencies, from 2020.
Noven Therapeutics, LLC recalls Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr), 30-count box, Rx only,, dated Mar 31, 2020. Every Noven Therapeutics, LLC recall is listed on this page, newest first.
The most common reasons on record: Defective Delivery System: Out of specification for mechanical peel and shear. (7).
Match the NDC and lot number on your bottle or box to the recall. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first. Report side effects to FDA MedWatch.
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