ConMed recalls
3 official recalls and safety alerts involving ConMed since 2022-12, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with ConMed or the relevant agency.
- 2026-09-02
USConMed Corporation recalls CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5.5mm GENESYs CrossFT Suture Anchor with two, #2 (5…
Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.
- 2026-06-24
- US
ConMed Corporation recalls ConMed AirSeal 12mm Access Port and Obturator with Blunt Tip, 100mm Length. Catalog Number: iASB12-100. 6 units per pack. Disposable…
Potential for overpressure alerts.
FDA · DeviceConMed CorporationNationwide distribution. International distribution to Australia, Austria,…Official notice → - 2022-12-21
- US
ConMed Corporation recalls Foot Controlled Electrosurgical Suction Coagulator, Electrosurgical Suction Coagulator 10FR, Catalog Number 130187
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…
FDA · DeviceConMed CorporationDomestic distribution nationwide. Foreign distribution to Colombia, Ecuador,…Official notice →