ConMed Corporation: 66 recalls on record

Recalls filed with 1 agency: FDA (66).

First recall on record: December 19, 2012. Most recent: September 2, 2026.

Risk classification: Class I: 9 · Class II: 57

Most recent recalls

DateAgencyProduct
August 31, 2016FDAAdult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.), 10' (3.05m) Cable, C…Z-2595-2016
December 10, 2014FDAADULT Radiotransparent Electrode, REF/Catalog Number 2001H, Rx ONLY --- COMPARABLE TO PHI…Z-0454-2015
December 10, 2014FDAADULT Radiotransparent Electrode, REF/Catalog Number 2001H-C, Rx ONLY --- COMPARABLE TO P…Z-0455-2015
December 10, 2014FDAMINI PEDIATRIC Radiotransparent Electrode, REF/Catalog Number 2602H, Rx ONLY --- COMPARAB…Z-0460-2015
December 10, 2014FDAADULT Radiotransparent Electrode, REF/Catalog Number 2001H-PC, Rx ONLY --- COMPARABLE TO …Z-0456-2015
December 10, 2014FDACONMED PEDIATRIC R2 Multifunction Electrodes, REF/Catalog Number 3115-1750, Direct Connec…Z-0461-2015
December 10, 2014FDAADULT Radiotransparent Electrode, REF/Catalog Number 2516H-PC, Rx ONLY --- COMPARABLE TO …Z-0458-2015
December 10, 2014FDACONMED ADULT R2 Multifunction Electrodes, REF/Catalog Number 3115-1751, Direct Connect to…Z-0462-2015
December 10, 2014FDAADULT Radiotransparent Electrode, REF/Catalog Number 2516H, Rx ONLY --- COMPARABLE TO PHI…Z-0457-2015
December 10, 2014FDAPEDIATRIC Radiotransparent Electrode, REF/Catalog Number 2603H, Rx ONLY --- COMPARABLE TO…Z-0459-2015
June 25, 2014FDAAltrus Thermal Tissue Fusion Handpieces under the following specifications: 1) 10mm x 16 …Z-1839-2014
June 11, 2014FDAMACROLYTE Premie Dispersive Electrode, REF 440-2400, CONMED CORPORATION. The device is …Z-1719-2014
November 27, 2013FDAALTRUS¿ THERMAL TISSUE FUSION, Tissue Fusion Handpiece, 5 mm O.D., 36 cm Shaft, REF 60-9…Z-0332-2014
November 27, 2013FDAALTRUS¿ THERMAL TISSUE FUSION, Tissue Fusion Handpiece, 5 mm O.D., 16 cm Shaft, REF 60-9…Z-0331-2014
May 22, 2013FDAPadPro(R) Adult Radiotransparent Multifunction Electrodes, REF/Catalog No. 2001M-C. T…Z-1317-2013
February 27, 2013FDAELECTROLASE HYFRECATOR(R) ELECTRODES - SHARP, REF/Catalog Number 7-100-8BX, Disposable Hy…Z-0826-2013
February 27, 2013FDAELECTROLASE(R) HYFRECATOR(R) ELECTRODES - BLUNT, REF/Catalog Number 7-101-8BX, Disposable…Z-0827-2013
January 30, 2013FDAUltraClean(R) Accessory Electrode 6 inch Coated Needle with Extended Insulation, REF/Cata…Z-0734-2013
January 30, 2013FDAUltraClean(R) Accessory Electrode 4 inch Coated Blade, REF/Catalog No. 139112, Single Us…Z-0736-2013
January 30, 2013FDAABC(R) NOZZLE, Single Patient Use Nozzle, (For use with 130500 Reusable ABC(R) Handpiece)…Z-0724-2013
January 30, 2013FDATUR/Endoscopic Cable, 10 feet (3.05 mm), REF/Catalog No. 135171, Disposable, Sterile, Rx …Z-0725-2013
January 30, 2013FDAElectrosurgical Tip Cleaner, REF/Catalog No. 138029, Single Use, Sterile, Rx ONLY -- Dist…Z-0728-2013
January 30, 2013FDAUltraClean(R) Accessory Electrode 6 inch Coated Blade with Extended Insulation, REF/Catal…Z-0735-2013
January 30, 2013FDACONMED(R) ELECTROSURGICAL SAFETY HOLSTER, Disposable Safety Holster, REF/Catalog No. 1376…Z-0726-2013
January 30, 2013FDAUltraClean(R) Accessory Electrode 1 inch Coated Needle with Extended Insulation, REF/Cata…Z-0732-2013

Questions about this company

How many recalls does ConMed Corporation have?
Recalert has 66 U.S. recalls on record for ConMed Corporation, published between December 19, 2012 and September 2, 2026.
Which agencies have handled ConMed Corporation recalls?
ConMed Corporation appears as the recalling firm in recalls from: FDA (66).

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