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.
Reported: March 29, 2023 Initiated: March 10, 2023 #D-0470-2023
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.
Reason for Recall
Defective Delivery System: Out of specification for shear.
Details
- Recalling Firm
- Noven Pharmaceuticals Inc
- Units Affected
- N/A
- Distribution
- US Nationwide
- Location
- Miami, FL
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Noven Pharmaceuticals Inc. Units affected: N/A.
Why was this product recalled? ▼
Defective Delivery System: Out of specification for shear.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on March 29, 2023. Severity: Moderate. Recall number: D-0470-2023.
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