CONMED STK190-127-90Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10845854020821), received between Aug 30, 2018 and Aug 30, 2018 — classified as 1 malfunction.

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 16, 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.

• MalfunctionAug 30, 2018Material Fragmentation; Material Fragmentation

  THE SALES REPRESENTATIVE REPORTED ON BEHALF OF THE CUSTOMER THAT THE STK190-127-90, STRYKER OSCILLATING SAW BLADE REPLACEMENT 19 MM X 1.27 MM (0.050 INCH) X 90 MM, QTY 5, DEVICE BROKE DURING A TOTAL KNEE ARTHROSCOPY PROCEDURE ON (B)(6) 2018. AT INITIAL REPORTING, IT WAS STATED THAT A PIECE OF THE DEVICE WAS LOST; HOWEVER, AFTER COMPLETION OF THE CUSTOMER COMPLAINT FORM DURING THE PROCEDURE THE PATIENT WAS X-RAYED AND THE FRAGMENT WAS FOUND AND REMOVED. TO COMPLETE THE PROCEDURE ANOTHER DEVICE WAS USED, AND THE PROCEDURE COMPLETED SUCCESSFULLY WITH A 5-MINUTE DELAY. THERE WAS NO REPORT OF INJURY TO THE PATIENT. THIS REPORT IS BEING RAISED ON THE BASIS OF MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7834323 ↗