ConMed Corporation

Complete recall history across all FDA and CPSC categories — 80 total recalls

ConMed Corporation appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (80)

FDA medical device enforcement actions by ConMed Corporation. Showing most recent 50.

Date Product Reason Class
Nov 18, 2022 Foot Controlled Electrosurgical Suction Coagulator, Electrosurgical Suction C... Suction ports may potentially be occluded on the affected devices. If this oc... Class II
Mar 26, 2021 INFINITY_TRAY Custom Procedural Kit - Canada. containing Infinity ACL Tibia... Tip Guides are potentially misaligned laterally which could affect the accura... Class II
Mar 26, 2021 KIT_INFINITY_BASE Custom Procedural Kit - Italy, containing Infinity ACL Tibi... Tip Guides are potentially misaligned laterally which could affect the accura... Class II
Nov 12, 2020 Infinity ACL Tibial Elbow Guide-indicated for use in open and arthroscopic pr... Tips of the Infinity ACL Tibial Elbow and Tip Guides are potentially misalign... Class II
Nov 12, 2020 Infinity ACL Tibial Tip Guide- indicated for use in open and arthroscopic pr... Tips of the Infinity ACL Tibial Elbow and Tip Guides are potentially misalign... Class II
Mar 21, 2019 ConMed Anchor Tissue Retrieval System", 12 MM, 300 ML (5/BX) Catalog Number:... Voids in the seal or a partial seal results in an open channel and may compro... Class II
Mar 21, 2019 ConMed Anchor Tissue Retrieval System, 8 MM, 125 ML (5/BX) Catalog Number:TR... Voids in the seal or a partial seal results in an open channel and may compro... Class II
Mar 21, 2019 ConMed Anchor Tissue Retrieval System, 15 MM, 1850 ML (3/BX) Catalog Number:... Voids in the seal or a partial seal results in an open channel and may compro... Class II
Mar 21, 2019 ConMed Anchor Tissue Retrieval System, VATS, 15 MM, 1550 ML (3/BX) Catalog N... Voids in the seal or a partial seal results in an open channel and may compro... Class II
Mar 21, 2019 ConMed Anchor Tissue Retrieval System 15 MM, 1550 ML (3/BX) Catalog Number: ... Voids in the seal or a partial seal results in an open channel and may compro... Class II
Mar 21, 2019 ConMed Anchor Tissue Retrieval System 10 MM, 235 ML, (5/BX) Catalog Number: ... Voids in the seal or a partial seal results in an open channel and may compro... Class II
Feb 23, 2018 MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Philips Plug Style Connector, ... Wire sets of certain devices were assembled with adhesive on the contact wire... Class II
Feb 23, 2018 MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, ZOLL¿ Connector, REF/Catalog N... Wire sets of certain devices were assembled with adhesive on the contact wire... Class II
Feb 23, 2018 MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Philips Plug Style Connector, ... Wire sets of certain devices were assembled with adhesive on the contact wire... Class II
Feb 23, 2018 MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Universal/Anderson Connector, ... Wire sets of certain devices were assembled with adhesive on the contact wire... Class II
Feb 23, 2018 MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Physio-Control¿ Quik-Combo" Co... Wire sets of certain devices were assembled with adhesive on the contact wire... Class II
Jun 19, 2017 STAT 2¿ I.V. Gravity Flow Needle-Free Controller Primary Administration Sets ... Intravascular (I.V.) fluid administration sets are exhibiting inaccurate or i... Class II
Jun 19, 2017 STAT 2¿ I.V. Gravity Flow Controller and STAT 2¿ Primary, Secondary Administr... Intravascular (I.V.) fluid administration sets are exhibiting inaccurate or i... Class II
Apr 17, 2017 Nonabsorbable suture anchor system intended to reattach soft tissue to bone i... Manufactured with the incorrect anchor outer body Class II
Feb 28, 2017 Sterile Handpiece Sheaths, P/N 7-796-19, included in the Accessory Packages c... For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons we... Class II
Feb 28, 2017 Sterile Handpiece Sheaths, P/N 7-796-19, included in the Accessory Packages c... For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons we... Class II
Feb 28, 2017 Sterile Handpiece Sheaths, P/N 7-796-19, included in the Accessory Packages c... For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons we... Class II
Feb 28, 2017 Sterile Handpiece Sheaths, P/N 7-796-19, included in the Accessory Packages c... For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons we... Class II
Feb 28, 2017 HYFRECATOR 2000 HANDPIECE SHEATH, REF/Part Number 7-796-19, Rx ONLY, STERILE,... For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons we... Class II
Aug 29, 2016 CONCEPT HEATWAVE Electrode 130 mm x 2.3 mm diameter, REF/Catalog Number CS-02... CONMED received complaints of damage to the CS-023 electrodes shaft insulati... Class II
Jun 27, 2016 CORE¿ Trumpet Handpiece with 5mm x 32cm Length Probe , Catalog Number CD8400 ... The packaging seal may contain a crease. The crease may result in an open ch... Class II
Jun 27, 2016 CORE¿ Suction Irrigation Handpiece Y-Tubing set, with 5mm x 32cm Length Probe... The packaging seal may contain a crease. The crease may result in an open ch... Class II
Jun 27, 2016 CORE¿ Suction Irrigation Handpiece without Probe for Single Solution or Dual ... The packaging seal may contain a crease. The crease may result in an open ch... Class II
Jun 27, 2016 CORE¿ Trumpet Handpiece only, Catalog Number CD8450 The CORE Trumpet (CD81XX... The packaging seal may contain a crease. The crease may result in an open ch... Class II
Jun 27, 2016 CORE¿ Suction Irrigation Handpiece with 5mm x 32cm Length Probe for Single So... The packaging seal may contain a crease. The crease may result in an open ch... Class II
Jun 27, 2016 CORE¿ Suction Irrigation Handpiece without Probe for Single Solution Bags, Ca... The packaging seal may contain a crease. The crease may result in an open ch... Class II
Jun 27, 2016 CORE¿ Suction Irrigation Handpiece with 5mm x 32cm Length Probe for Single So... The packaging seal may contain a crease. The crease may result in an open ch... Class II
May 18, 2016 Pediatric Dual Dispersive Electrodes (for patients 5-15 kg.), use with the Bi... A version of the dual dispersive electrodes may not be compatible with some e... Class II
May 18, 2016 Adult Dual Dispersive Electrodes (for patients >15 kg.), use with the Birtche... A version of the dual dispersive electrodes may not be compatible with some e... Class II
May 18, 2016 Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.), No Cable... A version of the dual dispersive electrodes may not be compatible with some e... Class II
May 18, 2016 Pediatric ThermoGard¿ Dual Dispersive Electrodes (for patients 5-15 kg.), 10'... A version of the dual dispersive electrodes may not be compatible with some e... Class II
May 18, 2016 Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.), 10' (3.0... A version of the dual dispersive electrodes may not be compatible with some e... Class II
Dec 21, 2015 Hip Preservation System Signature Series PreBent Burs under the following lab... Metal shavings released from burs during use are due to contact between the b... Class II
Nov 5, 2015 Altrus Thermal Tissue Fusion Energy Sources, Catalog Numbers: 1) 60-9500-120 ... Miscalibration of the Energy Source monitoring function, which may incorrectl... Class II
Jun 17, 2015 Arthroscopic Energy 50¿ Probe with Suction, Catalog number: AES-50S Peoduc... Probe programming error. The incorrect program can generate more heat at the... Class II
Nov 6, 2014 CONMED ADULT R2 Multifunction Electrodes, REF/Catalog Number 3115-1751, Direc... Philips Healthcare made changes to the design of the connection between multi... Class I
Nov 6, 2014 ADULT Radiotransparent Electrode, REF/Catalog Number 2001H, Rx ONLY --- COMPA... Philips Healthcare made changes to the design of the connection between multi... Class I
Nov 6, 2014 ADULT Radiotransparent Electrode, REF/Catalog Number 2516H-PC, Rx ONLY --- CO... Philips Healthcare made changes to the design of the connection between multi... Class I
Nov 6, 2014 PEDIATRIC Radiotransparent Electrode, REF/Catalog Number 2603H, Rx ONLY --- C... Philips Healthcare made changes to the design of the connection between multi... Class I
Nov 6, 2014 ADULT Radiotransparent Electrode, REF/Catalog Number 2001H-PC, Rx ONLY --- CO... Philips Healthcare made changes to the design of the connection between multi... Class I
Nov 6, 2014 ADULT Radiotransparent Electrode, REF/Catalog Number 2001H-C, Rx ONLY --- COM... Philips Healthcare made changes to the design of the connection between multi... Class I
Nov 6, 2014 CONMED PEDIATRIC R2 Multifunction Electrodes, REF/Catalog Number 3115-1750, D... Philips Healthcare made changes to the design of the connection between multi... Class I
Nov 6, 2014 MINI PEDIATRIC Radiotransparent Electrode, REF/Catalog Number 2602H, Rx ONLY ... Philips Healthcare made changes to the design of the connection between multi... Class I
Nov 6, 2014 ADULT Radiotransparent Electrode, REF/Catalog Number 2516H, Rx ONLY --- COMPA... Philips Healthcare made changes to the design of the connection between multi... Class I
May 8, 2014 MACROLYTE Premie Dispersive Electrode, REF 440-2400, CONMED CORPORATION. Th... ConMed Corporation has received complaints regarding sparking, no output and ... Class II

View all 80 device recalls →

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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