CONMED V190-119-90Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10845854021439), received between Dec 15, 2021 and Dec 15, 2021 — 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.

• MalfunctionDec 15, 2021Material Fragmentation; Material Fragmentation

  THE DISTRIBUTOR REPORTED ON BEHALF OF THEIR CUSTOMER THAT THE V190-119-90,OSCILLATING SAW BLADE WAS BEING USED ON AN UNKNOWN DATE SOMETIME DURING THE (B)(6), 2021 DURING A JOINT REPLACEMENT PROCEDURE WHEN IT WAS REPORTED ¿FOUND BROKEN METALLIC BIT ON TABLE AFTER SAW BLADE USE, CONFIRMED MISSING PIECES FROM SAW BLADE. RECOVERED 2 PIECES, CAN PUT ENTIRE BLADE BACK TOGETHER, NO MISSING PIECE. FLUOROSCOPY CONFIRMED NO METALLIC FB IN PATIENT.¿ THERE WAS NO REPORT OF IMPACT/INJURY TO THE PATIENT. THE PROCEDURE WAS COMPLETED WITHOUT AN ALTERNATE DEVICE. THIS REPORT IS BEING RAISED ON THE BASIS OF MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13009816 ↗