CONMED STK193-137-90Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10845854020838), received between Jul 31, 2019 and Jul 31, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Material Fragmentation” (1 report).

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. What reports can and can't tell you · How this data works · Data updated Oct 18, 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.

• InjuryJul 31, 2019Material Fragmentation; Material Fragmentation

  THIS DISTRIBUTOR REPORTED ON BEHALF OF THEIR CUSTOMER THAT THE STK193-137-90 DEVICE WAS USED DURING A TOTAL KNEE ARTHROPLASTY ON (B)(6) 2019. AFTER CLOSING THE PATIENT AN X-RAY WAS TAKEN AND IT WAS REPORTED THAT A MISSING CUTTING EDGE (TOOTH) OF THE DEVICE WAS FOUND. THE PATIENT WAS REOPENED, AND THE FRAGMENT WAS RETRIEVED. THERE WAS NO REPORT OF PATIENT INJURY, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. THIS REPORT IS BEING RAISED ON THE BASIS OF INJURY DUE TO THE NECESSITY TO REOPEN THE PATIENT AFTER SURGICAL SITE CLOSURE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8846237 ↗