Noven Pharmaceuticals Inc is recalling 8,559 cartons of Daytrana (methylphenidate transdermal system) patches. The recall affects the 10 mg strength (1.1 mg/hr) patches sold in 30-count cartons. The recall was issued because the patches may rip when opened or have a tight release liner that causes adhesive transfer, which can interfere with the proper application and use of the medication.
The defective delivery system can cause the patches to rip or fail to release from their liner correctly. This may prevent the consumer from applying the patch properly or result in an incomplete dose of the medication.
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Quantity: 8,559 cartons.
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response
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