Reported Mar 10, 2021 · Terminated

Daytrana (methylphenidate transdermal system) Delivers 20 mg over 9 hours (2.2 mg/hr) Contains: 30 Patches in a…

Noven Pharmaceuticals Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Noven Pharmaceuticals Inc · 11960 Sw 144th St · Miami, FL · 33186-6109

Is this the product you have?

  • Daytrana (methylphenidate transdermal system) Delivers 20 mg over 9 hours (2.2
  • mg/hr) Contains30 Patches in a foil-sealed polypropylene tray, packed in a paper carton, Rx only, Manufactured for Noven Therapeutics, LLC, Miami, FL, 33186, By Noven Pharmaceuticals, Inc., Miami, FL, 33186, NDC 68968-5554-3
Lot codes and dates
    • Lots #: 87580
    • Exp 4/2021
    • 87819
    • Exp 4/2021
    • 88244
    • Exp 6/2021
    • 88245
    • Exp 6/2021
    • 88532
    • Exp 06/2021 & 88533
    • Exp 7/2021
Amount recalled
786,900 patches

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Where it was sold

  • Nationwide

Why it was recalled

Defective Delivery System: Out of specification for mechanical peel.

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Jul 5, 2024 · Data as of Sep 19, 8:06 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.