LIBERATOR 25.50016Recalls & reported problems
Conmed Corporation · RASP LIBERATOR KNIFE II, 4.75 X 149 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 10845854024478), received between Mar 26, 2019 and Mar 26, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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
- Break1
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.
MalfunctionMar 26, 2019Break; Break
THE CUSTOMER REPORTED THE 25.50016, LIBERATOR RASP, BROKE DURING A BANKART PROCEDURE. THE TIP WAS RETRIEVED FROM THE PATIENT USING ARTHROSCOPIC GRASPERS. THE SURGERY WAS COMPLETED AS PLANNED. THERE WAS A DELAY IN SURGERY, THOUGH THE DELAY TIME WAS NOT REPORTED. THE PROCEDURE WAS COMPLETED USING ANOTHER RASP. PICTURES WERE PROVIDED OF THE BROKEN INSTRUMENT. 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 8453541 ↗
Other RASP devices
- ATTUNE 2545-00-048Depuy (Ireland) · RASP22 reports
- P.F.C. 85-3927Depuy (Ireland) · RASP11 reports
- DePuy Sythes 10-306-000Symmetry Medical Inc. · Rasp11 reports
- EXACT REVERSE FP FULL TOOTH RASP SSI005613Zimmer, Inc. · Rasp3 reports
- EXACT REVERSE FP FULL TOOTH RASP SSI005610Zimmer, Inc. · Rasp3 reports
- EXACT REVERSE FP FULL TOOTH RASP SSI005614Zimmer, Inc. · Rasp3 reports
- ALIF 389.156Synthes GmbH · RASP3 reports
- ALIF 03.808.101Synthes GmbH · RASP2 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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