Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Foot Controlled Electrosurgical Suction Coagulator Recalled by ConMed Corporation Due to Suction ports may potentially be occluded on the...
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
Foot Controlled Electrosurgical Suction Coagulator, Electrosurgical Suction Coagulator 10FR, Catalog Number 130187
Quantity: 23,700 US; 5,225 OUS
Why Was This Recalled?
Suction ports may potentially be occluded on the affected devices. If this occurs, the affected devices will not be able to perform the suction function during use, which could cause a delay in procedure and could require another device to be used.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About ConMed Corporation
ConMed Corporation has 69 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report