CONMED C2610Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20845854019389), received between Feb 23, 2026 and Feb 23, 2026 — classified as 1 injury.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryFeb 23, 2026Adverse Event Without Identified Device or Use Problem

  CONMED JAPAN REPORTED ON BEHALF OF A CUSTOMER THAT THE C2610, CANCELLOUS SCREW, 6.5 X 25 MM DEVICE WAS USED IN AN ACL RECONSTRUCTION SURGERY ON AN UNKNOWN DATE AND IT WAS FOUND POST-OPERATIVELY THAT ¿A PATIENT WHO WAS TREATED USING OUR PRODUCT (CANCELLOUS SCREW 6.5 MM) IN COMBINATION WITH THE SMITH & NEPHEW ENDOBUTTON IS REPORTEDLY EXPERIENCING SOME KIND OF ABNORMALITY IN THE SKIN AROUND THE KNEE WHERE THE IMPLANT WAS PLACED¿. AT PRESENT, IT IS UNCLEAR WHETHER THE OBSERVED CONDITION IS DIRECTLY RELATED TO THE IMPLANTED DEVICES. HOWEVER, THE CURRENT SITUATION SUGGESTS THAT IT WOULD MORE LIKELY BE RELATED TO THE PATIENT¿S INDIVIDUAL SENSITIVITY OR BIOLOGICAL RESPONSE TO THE IMPLANT MATERIAL, RATHER THAN TO A PRODUCT DEFECT.¿. THE PROCEDURE WAS COMPLETED WITHOUT THE USE OF AN ALTERNATE DEVICE, AND WITH NO INTRA-OPERATIVE ISSUES REPORTED. TO DATE, THERE IS NO REPORT OF MEDICAL/SURGICAL INTERVENTION, OR EXTENDED HOSPITALIZATION FOR THE PATIENT. FURTHER INFORMATION WAS REQUESTED BUT WAS NOT MADE AVAILABLE. IT WAS REPORTED THAT DEVICE REMOVAL "IS EXPECTED TO BE CONSIDERED IN THE FUTURE, BUT THE DETAILS ARE UNKNOWN". THIS REPORT IS BEING RAISED DUE TO THE REPORTED INJURY OF AN UNDEFINED SK

  Patient problems: Insufficient Information

  MAUDE report 24414623 ↗