Overview of recall records associated with Conmed Corporation, including dates, categories and classifications where available.
Classification mix: Class II: 30.
Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.
Potential for overpressure alerts.
Potential for overpressure alerts.
Potential for overpressure alerts.
Potential for overpressure alerts.
Potential for overpressure alerts.
Potential for overpressure alerts.
Potential for overpressure alerts.
Potential for overpressure alerts.
Potential for overpressure alerts.
Potential for overpressure alerts.
Potential for overpressure alerts.
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…
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…
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…
Tips of the Infinity ACL Tibial Elbow and Tip Guides are potentially misaligned laterally which could affect the accuracy of the guide system
Tips of the Infinity ACL Tibial Elbow and Tip Guides are potentially misaligned laterally which could affect the accuracy of the guide system
Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
Wire sets of certain devices were assembled with adhesive on the contact wires, which may impede conductivity and could cause failure
This page summarizes recall records in which the official source identifies Conmed Corporation as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
