CONMED V130-089-90Recalls & reported problems
Conmed Corporation · OSCILLATING SAW BLADE 13 X 0.89 X 90 MM · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10845854021293), received between Jan 6, 2026 and Jan 6, 2026 — 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.
Reports received per month
Most reported problems
Device problems
- Material Fragmentation1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 6, 2026Material Fragmentation
CONMED KOREA REPORTED ON BEHALF OF THE CUSTOMER THAT THE V130-089-90 OSCILLATING SAW BLADE 13 X 0.89 X 90 MM DEVICE, WAS BEING USED DURING A TOTAL KNEE ARTHROPLASTY PROCEDURE ON (B)(6) 2025 WHEN IT WAS REPORTED, ¿THE HANDPIECE CONNECTION PORTION OF THE SAW BLADE USED DURING TOTAL KNEE ARTHROPLASTY FRACTURED. THE BROKEN FRAGMENT WAS HANDLED ACCORDING TO THE COUNT DISCREPANCY PROCEDURE, AND THE FRAGMENT WAS FOUND ON THE OPERATING ROOM FLOOR. IT IS ASSUMED THAT THE BLADE FRACTURED DURING SAWING AND THAT THE FRAGMENT WAS EJECTED OUTSIDE THE SURGICAL FIELD. THE COMPLAINT PRODUCT AND THE FRAGMENT WERE DISCARDED BY THE HOSPITAL. NO FRAGMENTS REMAINED IN THE PATIENT'S BODY. THERE WAS AN APPROXIMATE 2 MIN DELAY IN THE SURGERY. A REPLACEMENT PRODUCT WAS USED TO COMPLETE THE SURGERY SUCCESSFULLY, AND THE PATIENT'S CONDITION WAS STABLE.¿. FURTHER ASSESSMENT QUESTIONING FOUND THAT THE CUSTOMER HAS CONFIRMED THAT NO FRAGMENT WAS FOUND INSIDE OF THE PATIENT¿S BODY BUT JUST FOUND IT ON THE FLOOR. THE PROCEDURE WAS COMPLETED AND THERE WAS NO REPORT OF INJURY, MEDICAL INTERVENTION, OR EXTENDED HOSPITALIZATION FOR THE PATIENT. HOWEVER, CONMED KOREA HAS DECIDED TO REPORT THIS EVENT TO THEIR HEALTH AUT
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23978200 ↗
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- NA 0277096275Stryker Corporation · BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL72 reports
- Arthrex® AR-7300DSArthrex, Inc. · BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL70 reports
- NA 0277096277Stryker Corporation · BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL69 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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