Noven Therapeutics, LLC recalls Daytrana (methylphenidate transdermal system) Delivers 20 mg over 9 hours (2.2 mg/hr) 30-count box, Rx only, Manufactur…
- Recall date
- March 31, 2020
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-1248-2020
- FDA classification
- Class II
- Brand / firm
- Noven Therapeutics, LLC
- Sold / distributed
- Distributed Nationwide in the US
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) Delivers 20 mg over 9 hours (2.2 mg/hr) 30-count box, Rx only, Manufactured for Noven Therapeutics, LLC Miami, FL 33186, NDC 68968-5554-3
Get recall alerts
Free email alert whenever Noven Therapeutics, LLC has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Noven Therapeutics, LLC