Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Clonidine Transdermal System Recalled by Mayne Pharma Inc Due to Defective Delivery System: Out of specification for release...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Mayne Pharma Inc directly.
Affected Products
Clonidine Transdermal System, USP 0.3 mg/day, 4 Patches (NDC 51862-455-01) per Carton (51862-455-04), Rx only, Manufactured for: Mayne Pharma Greenville, NC 27834
Quantity: 1440 cartons
Why Was This Recalled?
Defective Delivery System: Out of specification for release liner removal force results at the 3-month CRT stability timepoint.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Mayne Pharma Inc
Mayne Pharma Inc has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report