CONMED 25.50014Recalls & reported problems
Conmed Corporation · LIBERATOR KNIFE, 4.5 MM X 150 MM · Class 1
Data updated Oct 16, 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 10845854024461), received between Feb 7, 2019 and Feb 7, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fracture” (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
Device problems
- Fracture1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 7, 2019Fracture; Fracture
THE CUSTOMER REPORTED THAT THE 25.50014, 4.5MM LIBERATOR KNIFE BROKE DURING A SLAP REPAIR ON (B)(6) 2018. IT'S REPORTED THE " TIP PART WAS BROKEN AFTER THE SURGEON WAS ISOLATING LABRUM FROM HUMERAL HEAD. THE BROKEN PIECE FELL INSIDE OF A PATIENT'S BODY, BUT IT WAS REMOVED USING GRASPER. SURGERY WAS COMPLETED SUCCESSFULLY WITHOUT AN ALTERNATE DEVICE." THERE WAS NO REPORTED PATIENT INJURY AND A 1-MINUTE REPORTED DELAY OF SURGERY. THIS REPORT IS BEING RAISED BASED ON DEVICE MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8318151 ↗
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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