ConMed Recalls
91 recalls on record · December 19, 2012 to June 24, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
June 24, 2026Medical DevicesFDA
ConMed Corporation recalls ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS12-
Hazard: Potential for overpressure alerts.
June 24, 2026Medical DevicesFDA
ConMed Corporation recalls ConMed AirSeal 12mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm Length. Catalog Number: iAS1
Hazard: Potential for overpressure alerts.
June 24, 2026Medical DevicesFDA
ConMed Corporation recalls ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip, 150mm Length. Catalog Number: iAS12-
Hazard: Potential for overpressure alerts.
June 24, 2026Medical DevicesFDA
ConMed Corporation recalls ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS5-
Hazard: Potential for overpressure alerts.
June 24, 2026Medical DevicesFDA
ConMed Corporation recalls ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm Length. Catalog Number: iAS5-
Hazard: Potential for overpressure alerts.
June 24, 2026Medical DevicesFDA
ConMed Corporation recalls ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 75mm Length. Catalog Number: iAS5-7
Hazard: Potential for overpressure alerts.
June 24, 2026Medical DevicesFDA
ConMed Corporation recalls ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS8-
Hazard: Potential for overpressure alerts.
June 24, 2026Medical DevicesFDA
ConMed Corporation recalls ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm Length. Catalog Number: iAS8-
Hazard: Potential for overpressure alerts.
June 24, 2026Medical DevicesFDA
ConMed Corporation recalls ConMed AirSeal 12mm Access Port and Obturator with Blunt Tip, 100mm Length. Catalog Number: iASB12-100. 6 units per pack
Hazard: Potential for overpressure alerts.
June 24, 2026Medical DevicesFDA
ConMed Corporation recalls ConMed AirSeal 12 mm Access Port and Obturator with Blunt Tip, 120mm Length. Catalog Number: iASB12-120. 6 units per pac
Hazard: Potential for overpressure alerts.
June 24, 2026Medical DevicesFDA
ConMed Corporation recalls ConMed AirSeal 5 mm Smooth Access Port and Obturator with Blunt Tip, 150mm Length. Catalog Number: iASB5-150. 6 units pe
Hazard: Potential for overpressure alerts.
December 21, 2022Medical DevicesFDA
ConMed Corporation recalls Foot Controlled Electrosurgical Suction Coagulator, Electrosurgical Suction Coagulator 10FR, Catalog Number 130187
Hazard: 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.
May 5, 2021Medical DevicesFDA
ConMed Corporation recalls KIT_INFINITY_BASE Custom Procedural Kit - Italy, containing Infinity ACL Tibial Elbow and Tip Guides product line, KTE10
Hazard: Tip Guides are potentially misaligned laterally which could affect the accuracy of the guide system and could cause a delay in procedure and may require another device or alternate surgical method to be used
May 5, 2021Medical DevicesFDA
ConMed Corporation recalls INFINITY_TRAY Custom Procedural Kit - Canada. containing Infinity ACL Tibial Elbow and Tip Guides product line, KTE100
Hazard: Tip Guides are potentially misaligned laterally which could affect the accuracy of the guide system and could cause a delay in procedure and may require another device or alternate surgical method to be used
December 30, 2020Medical DevicesFDA
ConMed Corporation recalls Infinity ACL Tibial Tip Guide- indicated for use in open and arthroscopic procedures for knee ligament reconstruction.
Hazard: Tips of the Infinity ACL Tibial Elbow and Tip Guides are potentially misaligned laterally which could affect the accuracy of the guide system
December 30, 2020Medical DevicesFDA
ConMed Corporation recalls Infinity ACL Tibial Elbow Guide-indicated for use in open and arthroscopic procedures for knee ligament reconstruction.
Hazard: Tips of the Infinity ACL Tibial Elbow and Tip Guides are potentially misaligned laterally which could affect the accuracy of the guide system
May 15, 2019Medical DevicesFDA
Conmed Corporation recalls ConMed Anchor Tissue Retrieval System", 12 MM, 300 ML (5/BX) Catalog Number: TRS-ROBO-12 The Anchor Tissue Retrieva
Hazard: Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
May 15, 2019Medical DevicesFDA
Conmed Corporation recalls ConMed Anchor Tissue Retrieval System, 8 MM, 125 ML (5/BX) Catalog Number:TRS-ROBO-8 The Anchor Tissue Retrieval Sy
Hazard: Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
May 15, 2019Medical DevicesFDA
Conmed Corporation recalls ConMed Anchor Tissue Retrieval System, VATS, 15 MM, 1550 ML (3/BX) Catalog Number: TRS-VATS-15 The Anchor Tissue Re
Hazard: Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
May 15, 2019Medical DevicesFDA
Conmed Corporation recalls ConMed Anchor Tissue Retrieval System, 15 MM, 1850 ML (3/BX) Catalog Number:TRS190SB2 The Anchor Tissue Retrieval S
Hazard: Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
May 15, 2019Medical DevicesFDA
Conmed Corporation recalls ConMed Anchor Tissue Retrieval System 15 MM, 1550 ML (3/BX) Catalog Number: TRS175SB2 The Anchor Tissue Retrieval S
Hazard: Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
May 15, 2019Medical DevicesFDA
Conmed Corporation recalls ConMed Anchor Tissue Retrieval System 10 MM, 235 ML, (5/BX) Catalog Number: TRS100SB2 The Anchor Tissue Retrieval S
Hazard: Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
April 4, 2018Medical DevicesFDA
ConMed Corporation recalls MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, ZOLL¿ Connector, REF/Catalog Number 2602Z Indicated for use in extern
Hazard: Wire sets of certain devices were assembled with adhesive on the contact wires, which may impede conductivity and could cause failure
April 4, 2018Medical DevicesFDA
ConMed Corporation recalls MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Physio-Control¿ Quik-Combo" Connector, REF/Catalog Number 2602M Indic
Hazard: Wire sets of certain devices were assembled with adhesive on the contact wires, which may impede conductivity and could cause failure
April 4, 2018Medical DevicesFDA
ConMed Corporation recalls MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Philips Plug Style Connector, REF/Catalog Number 2602H Indicated for
Hazard: Wire sets of certain devices were assembled with adhesive on the contact wires, which may impede conductivity and could cause failure
April 4, 2018Medical DevicesFDA
ConMed Corporation recalls MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Philips Plug Style Connector, REF/Catalog Number 2602H Indicated for
Hazard: Wire sets of certain devices were assembled with adhesive on the contact wires, which may impede conductivity and could cause failure
April 4, 2018Medical DevicesFDA
ConMed Corporation recalls MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Universal/Anderson Connector, REF/Catalog Number 2602 Indicated for us
Hazard: Wire sets of certain devices were assembled with adhesive on the contact wires, which may impede conductivity and could cause failure
March 7, 2018Medical DevicesFDA
ConMed Corporation recalls STAT 2¿ I.V. Gravity Flow Needle-Free Controller Primary Administration Sets and Extension Sets (Catalog Numbers: (1) S2
Hazard: Intravascular (I.V.) fluid administration sets are exhibiting inaccurate or inconsistent flow rates.
March 7, 2018Medical DevicesFDA
ConMed Corporation recalls STAT 2¿ I.V. Gravity Flow Controller and STAT 2¿ Primary, Secondary Administration Sets and Extension Sets (Catalog Numb
Hazard: Intravascular (I.V.) fluid administration sets are exhibiting inaccurate or inconsistent flow rates.
December 20, 2017Medical DevicesFDA
ConMed Corporation recalls Nonabsorbable suture anchor system intended to reattach soft tissue to bone in orthopedic surgical procedures may be use
Hazard: Manufactured with the incorrect anchor outer body