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CONMED V190-127-05Recalls & reported problems

Conmed Corporation · OSCILLATING SAW BLADE 19 X 1.27 X 105 MM · Class 1

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10845854021446), received between Apr 5, 2023 and Apr 5, 2023 — 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

Device problems

  • Material Fragmentation1

Patient problems

  • Foreign Body In Patient1

Recent adverse event reports

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

  • InjuryApr 5, 2023Material Fragmentation; Material Fragmentation

    THE SALES REPRESENTATIVE REPORTED ON BEHALF OF THE CUSTOMER THAT THE V190-127-05 OSCILLATING SAW BLADE 19 X 1.27 X 105MM QTY 5 WAS BEING USED ON (B)(6) 2023 DURING A TOTAL HIP REPLACEMENT PROCEDURE AND ¿THE CUTTING EDGE OF THE BLADE WAS DAMAGED DURING THE FIRST FEMORAL CUT (NEW PACKAGING - ONE CUT).¿ AFTER FURTHER ASSESSMENT IT WAS FOUND THE BLADE DID FRAGMENT (THE LATERAL TOOTH BROKE OFF) AND THE "NURSES DISCOVERED THE SITUATION AT THE END OF THE SURGERY (PATIENT SKIN ALREADY CLOSED). THEY DIDN¿T FIND THE BLADE PIECE, THEY INFORMED THE SURGEON WHO DECIDED TO NO TAKE OTHER ACTIONS." IT IS UNKNOWN IF THE FRAGMENT FELL INTO THE SURGICAL SITE, "THEY ARE NOT SURE BECAUSE THEY DIDN¿T FIND THE FRAGMENTED PIECE ANYMORE. PROBABLY IT FELL OUTSIDE THE SURGICAL SITE, BUT THEY DIDN'T GIVE ME A DEFINITIVE ANSWER. THEY DIDN'T DO RX CONTROL." THE PROCEDURE WAS COMPLETED AND THERE WAS NO DELAY. THE PATIENT WAS REPORTED AS "OK" AND THERE WAS NO MEDICAL/SURGICAL INTERVENTION OR PROLONGED HOSPITALIZATION REQUIRED. THIS REPORT IS BEING RAISED ON THE BASIS OF INJURY DUE TO FRAGMENTATION, ALTHOUGH THEY ARE NOT CERTAIN IT FELL INTO THE SURGICAL SITE, THEY CANNOT PRODUCE THE PIECE AND ITS LOCATION IS UNKN

    Patient problems: Foreign Body In Patient

    MAUDE report 16683997 ↗

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Sources and updates

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