Every recall we track for ConMed Corporation — 30 in all — plus the complaints and injury reports the public filed about them.
ConMed recalls 5.5mm GENESYS CrossFT Suture Anchors with possible incorrect patient implant cards, risking wrong device identification. Affected units have specific reference numbers.
ConMed recalls 100mm AirSeal 12mm Access Port with Palm Grip Obturator due to potential overpressure alerts. Affected units have specific catalog numbers and lot numbers from June 2024 to January 2026.
ConMed recalls 6 units of AirSeal 12mm Access Port with potential overpressure alerts. Affected units have specific catalog and lot numbers. Consumers should contact ConMed for details.
ConMed recalls 6-unit packs of AirSeal 5mm Access Port with potential overpressure alerts. Affected items have specific catalog numbers and lot dates. Consumers should contact ConMed for details.
ConMed recalls 60+ units of AirSeal 5mm Access Port with potential overpressure alerts. Learn how to identify and stop using affected products.
ConMed recalls 150mm AirSeal 12mm Access Port with potential overpressure alerts. 6 units per pack, catalog number iAS12-150LPI. Affected units manufactured June 2024-January 2026.
ConMed recalls 120mm AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip (Catalog iAS8-120LP) due to potential overpressure alerts. 6 units per pack, manufactured June 2024-January 2026.
ConMed recalls 6-unit packs of AirSeal 8mm Access Port with potential overpressure alerts. Affected units have specific catalog numbers and lot dates from June 2024 to January 2026.
ConMed recalls 6 units of AirSeal 5mm Smooth Access Port with potential overpressure alerts. Affected units have specific catalog numbers and production dates. Consumers should contact ConMed for details.
ConMed recalls 12mm AirSeal Access Ports with potential overpressure alerts. Affected units have specific catalog numbers and lot dates from June 2024 to January 2026.
ConMed recalls 6-unit packs of AirSeal 5mm Access Port with potential overpressure alerts. Catalog number iAS5-100LP. Lot numbers from 202406204 to 202509244. Check your device for these numbers.
ConMed recalls 12mm AirSeal Access Ports with potential overpressure alerts. Affected units have specific catalog numbers and production dates. Consumers should contact ConMed for details.
ConMed recalls Electrosurgical Suction Coagulators 10FR with potential suction port occlusion, risking procedure delays. Affected units have specific lot codes and catalog numbers.
ConMed recalls Infinity Tray Custom Procedural Kits (KTE100/KTT100) for possible lateral misalignment affecting surgical accuracy. Affected units sold in Canada with serial numbers 001, 005.
ConMed recalls certain KIT_INFINITY_BASE Custom Procedural Kits for possible lateral misalignment of tip guides, which may delay surgery or require alternative procedures.
ConMed recalls Infinity ACL Tibial Elbow Guide for potential misalignment of tips, which could affect surgical accuracy during knee ligament reconstruction procedures.
ConMed recalls Infinity ACL Tibial Tip Guides for possible lateral misalignment during knee ligament surgery. Affected units have specific catalog numbers and lot codes. Contact ConMed for details.
ConMed recalls surgical tissue retrieval pouches (TRS-ROBO-12) manufactured between April 2018 and February 2019 due to potential sterility compromise from seal defects.
ConMed recalls Anchor Tissue Retrieval System (8mm, 125ml) manufactured between April 2018 and February 2019 due to potential sterility compromise. Affected units have specific lot codes.
ConMed recalls sterile surgical pouches (TRS190SB2) manufactured April 2018-Feb 2019 that may have compromised sterility due to seal defects, risking infection during laparoscopic surgery.
ConMed recalls certain Anchor Tissue Retrieval Systems (VATS, 15mm) due to potential seal failure causing sterility issues. Affected units manufactured from April 2018 to February 2019 with specific lot codes.
ConMed recalls sterile surgical pouches with potential sterility compromise due to seal defects. Affected units manufactured April 2018 to February 2019; check lot codes for exclusions.
ConMed recalls specific surgical pouches due to potential sterility compromise from seal defects. Affected units manufactured between April 2018 and February 2019 with certain lot codes.
ConMed recalls Mini Infant <3kg Radiotranslucent Electrodes with adhesive on contact wires that may cause failure. Affected units have specific lot numbers. Stop using immediately.
ConMed recalls pediatric electrodes with adhesive on contact wires that may cause failure. Affected units have specific lot numbers and are used for infant defibrillation. Stop using immediately if you have the product.
ConMed recalls Mini Infant < 3kg electrodes with adhesive on contact wires that may cause device failure. Affected units have specific lot numbers and are used for pediatric cardiac monitoring.
ConMed recalls infant electrodes with adhesive on contact wires that may impede conductivity and cause device failure. Affected units have specific lot numbers and are used for pediatric cardiac monitoring.
ConMed recalls Mini Infant < 3kg Radiotranslucent Electrodes with adhesive on contact wires that may impede conductivity and cause device failure. Affected units include specific lot numbers.
