Daytrana recall
Daytrana (methylphenidate transdermal system), Delivers 10 mg over 9 hours (1.1 mg/hr), Contains: 30 Patches in a foil-sealed polypropylene tray…
Why was Daytrana recalled?
Defective Delivery System: Out of specification for mechanical peel.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lots #: 87579, Exp 3/2021 & 88243, Exp 7/2021.
- Product
- Daytrana (methylphenidate transdermal system), Delivers 10 mg over 9 hours (1.1 mg/hr), Contains: 30 Patches in a foil-sealed polypropylene tray…
- Recalling firm
- Noven Pharmaceuticals Inc
- Quantity
- 473,280 patches
- Distribution
- Nationwide in the USA
- Recall date
- March 10, 2021
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)