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Class II: temporary or reversible health riskOngoing

Noven Pharmaceuticals Daytrana Recall

Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1

Noven Pharmaceuticals Inc · Miami, FL

Risk level
Class II
Reported by FDA
Jul 6, 2022
Recall ID
D-1169-2022
Check your lot numberHow we source this data

Summary

Noven Pharmaceuticals recalled Daytrana starting Jun 24, 2022. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1169-2022 on Jul 6, 2022. Reason: Defective Delivery System: Customer complaints received for ripping patches and tight release/adhesive transfer. Status: Ongoing.

Why it was recalled

Defective Delivery System: Customer complaints received for ripping patches and tight release/adhesive transfer.

Product description

Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr) Contains: 30 Patches, Rx only, Manufactured for Noven Therapeutics, LLC, Miami, FL 33186 By Noven Pharmaceuticals, Inc., Miami, FL 33186. NDC 68968-5552-3

Lot numbers, UPCs & expiration codes

Lot: 91272 Exp. 12/22.

Where it was sold

Distributed Nationwide in the USA

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-1169-2022
Classification
Class II
Status
Ongoing
Recall initiated
Jun 24, 2022
FDA report date
Jul 6, 2022
Quantity
8,559 cartons
Recall type
Voluntary: Firm initiated
Recalling firm
Noven Pharmaceuticals Inc

Original FDA data

Every field from FDA enforcement report D-1169-2022, exactly as published.

Show all FDA fields
City
Miami
State
FL
Status
Ongoing
Country
United States
Event ID
90506
Address
11960 Sw 144th St
Code information
Lot: 91272 Exp. 12/22.
Postal code
33186-6109
Report date
Jul 6, 2022
Product type
Drugs
Recall number
D-1169-2022
Classification
Class II
Recalling firm
Noven Pharmaceuticals Inc
Product quantity
8,559 cartons
Reason for recall
Defective Delivery System: Customer complaints received for ripping patches and tight release/adhesive transfer.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr) Contains: 30 Patches, Rx only, Manufactured for Noven Therapeutics, LLC, Miami, FL 33186 By Noven Pharmaceuticals, Inc., Miami, FL 33186. NDC 68968-5552-3
Distribution pattern
Distributed Nationwide in the USA
Recall initiation date
Jun 24, 2022
Initial firm notification
Letter
Center classification date
Jun 29, 2022

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1169-2022, published Jul 6, 2022. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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