Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.) Recalled by Conmed Corporation Due to A version of the dual dispersive electrodes may...
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 Conmed Corporation directly.
Affected Products
Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.), 10' (3.05m) Cable, Catalog Number 51-7310. Intended to be used for the dispersion and return to the electrosurgical generator.
Quantity: 307,684 units
Why Was This Recalled?
A version of the dual dispersive electrodes may not be compatible with some electrosurgical generators, placing patients at risk for undetected pad lift and a potential burn.
Where Was This Sold?
This product was distributed to 44 states: AL, AK, AZ, AR, CA, CO, CT, FL, GA, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NE, NV, NJ, NM, NY, NC, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WV, WI, WY
About Conmed Corporation
Conmed Corporation has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report