Noven Therapeutics, LLC recalls Daytrana (methylphenidate transdermal system) patches, Delivers 15 mg over 9 hours (1.6 mg/hr), 30-count box, Rx only,…
- Recall date
- March 2, 2020
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-1043-2020
- FDA classification
- Class II
- Brand / firm
- Noven Therapeutics, LLC
- Sold / distributed
- U.S.A. Nationwide
Why it was recalled
Defective Delivery System: Out of specification for mechanical peel and shear.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Daytrana (methylphenidate transdermal system) patches, Delivers 15 mg over 9 hours (1.6 mg/hr), 30-count box, Rx only, Manufactured for Noven Therapeutics, LLC. Miami, FL 33186, NDC 68968-5553-3
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