Daytrana recall
Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr) Contains: 30 Patches, Rx only, Manufactured for Noven…
Why was Daytrana recalled?
Defective Delivery System: customer complaints exceeded respective action limits.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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?
Lot: 90764 Exp. 08/2022
- Product
- Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr) Contains: 30 Patches, Rx only, Manufactured for Noven…
- Recalling firm
- Noven Pharmaceuticals Inc
- Quantity
- 274, 110 patches
- Distribution
- Nationwide to the U.S. Market
- Recall date
- June 1, 2022
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (drug)