Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Tourni-Cot - Universal Recalled by Mar-Med Co Due to A failure can occur if the user attempts...
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 Mar-Med Co directly.
Affected Products
Tourni-Cot - Universal, UDI 00855364004085, Model Number TCU, Non-pneumatic Tourniquet - Product Usage: The device is intended to be used in surgery on fingers or toes to provide a blood-less field.
Quantity: 52,000
Why Was This Recalled?
A failure can occur if the user attempts to remove the device by partially snipping the edge and pulling on it. The device may tear into two pieces with a portion remaining in place, which can continue to constrict the vessels. This type of failure can result in digit ischemia.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Mar-Med Co
Mar-Med Co has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report