Daytrana (methylphenidate transdermal system) CII, 10mg, 30-count carton, Rx only, Manufactured for Noven Therapeutics,
Summary
The FDA issued a Class II for Daytrana (methylphenidate transdermal system) CII, 10mg, 30-count carton, Rx onl by Noven Pharmaceuticals Inc. Reason: Defective Delivery System: Out of specification for shear..
Details
Source
Drug Recall
External ID
D-0470-2023
Action Date
2023-03-29
Status
Ongoing
Category
drug
Product Description
Daytrana (methylphenidate transdermal system) CII, 10mg, 30-count carton, Rx only, Manufactured for Noven Therapeutics, LLC., Miami by Noven Pharmaceuticals, Inc., NDC 68968-5552-3.
Lot/Code Info: Lot#: 91955, Exp. 7/2023; 93039, Exp. 10/2023
Quantity Affected: N/A
Reason for Recall
Defective Delivery System: Out of specification for shear.
Distribution
US Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2023-03-10
Company
Miami, FL
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 40 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
Noven Pharmaceuticals Inc has 10 FDA actions in our database, including 10 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Noven Pharmaceuticals Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Noven Pharmaceuticals Inc have FDA actions?
Noven Pharmaceuticals Inc has 10 FDA actions in our database, including 10 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0470-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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