Innomed, Inc. 3004-01Recalls & reported problems
Innomed, Inc. · Unger Canal Finder Rasp Curved · 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 00840277104960), received between Jun 1, 2024 and Jun 1, 2024 — 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.
Reports received per month
Most reported problems
Device problems
- Break1
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 1, 2024Break; Break
IT WAS REPORTED THAT RASP BECAME STUCK IN FEMUR. SURGEON APPLIED MORE FORCE AND THE HANDLE SEPARATED FROM RASP. THIS REPORT REFLECTS INFORMATION RECEIVED BY FDA IN THE FORM OF A NOTIFICATION. PROCEDURE: TOTAL HIP REPLACEMENT.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 19442052 ↗
Other Rasp, Surgical, General & Plastic Surgery devices
- Progressive proximal rasp PIP 211-A43000Keri Medical SA · Rasp, Surgical, General & Plastic Surgery4 reports
- VG2 273340107Medos International Sàrl · RASP, SURGICAL, GENERAL & PLASTIC SURGERY2 reports
- VG2 273340106Medos International Sàrl · RASP, SURGICAL, GENERAL & PLASTIC SURGERY2 reports
- VG2 273340108Medos International Sàrl · RASP, SURGICAL, GENERAL & PLASTIC SURGERY1 report
- NA 698273327Depuy Spine, LLC · RASP, SURGICAL, GENERAL & PLASTIC SURGERY1 report
- CONCORDE 287903001Depuy Spine, LLC · RASP, SURGICAL, GENERAL & PLASTIC SURGERY1 report
- CONCORDE 287903003Depuy Spine, LLC · RASP, SURGICAL, GENERAL & PLASTIC SURGERY1 report
- VG2 273340110Medos International Sàrl · RASP, SURGICAL, GENERAL & PLASTIC SURGERY1 report
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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