CONMED V190-119-05Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10845854021422), received between May 9, 2024 and May 9, 2024 — 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 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.

• MalfunctionMay 9, 2024Material Fragmentation; Material Fragmentation

  THE SALES REPRESENTATIVE REPORTED ON BEHALF OF THE CUSTOMER THAT THE DEVICE V190-119-05, OSCILLATING SAW BLADE 19 X 1.19 X 105MM QTY 5, WAS BEING USED DURING A KNEE TEP PROCEDURE ON (B)(6) 2024 WHEN IT WAS REPORTED, ¿A TOOTH OF THE SAW BLADE BROKE OFF DURING THE SAWING PROCESS.". THERE WAS NO REPORT OF INJURY, MEDICAL INTERVENTION, OR HOSPITALIZATION FOR THE PATIENT. FURTHER ASSESSMENT QUESTIONS WERE ASKED AND IT WAS DISCOVERED THAT THE TOOTH OF THE SAW BLADE BROKE OFF AND AFTER A SHORT SEARCH IT WAS RECOVERED FROM THE OPERATING FIELD USING A CLAMP. IT IS UNKNOWN IF THE FRAGMENTATION HAD BEEN IN CONTACT WITH THE PATIENT. THE PROCEDURE WAS COMPLETED USING ANOTHER SAME DEVICE WHICH CAUSED A 5-MINUTE DELAY. THIS REPORT IS BEING RAISED DUE TO THE REPORTED MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE. UPDATE: ADDITIONAL INFORMATION RECEIVED 13MAY2024 STATES, "YES THE FRAGMENT WAS IN THE PATIENT AND COULD BE SECURED."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19276748 ↗