DePuy Sythes 10-306-000Recalls & reported problems
Symmetry Medical Inc. · IM CANAL FINDER · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 11
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 11 adverse event reports that list this exact device (DI 00847538010664), received between Apr 11, 2023 and Sep 14, 2026 — classified as 11 malfunctions.
The most frequently reported specific device problem is “Material Integrity Problem” (11 reports).
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 Integrity Problem11
Patient problems
- No Clinical Signs, Symptoms or Conditions11
Recent adverse event reports
The 11 most recent of 11 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 14, 2026Material Integrity Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50762661 ↗MalfunctionSep 14, 2026Material Integrity Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50760685 ↗MalfunctionJun 26, 2026Material Integrity Problem
IT WAS REPORTED THAT THE MATTA IM CANAL FINDER TIP BROKE WHEN THE DOCTOR WAS TRYING TO ENTER THE FEMUR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25636196 ↗MalfunctionJun 3, 2026Material Integrity Problem
IT WAS REPORTED THAT IT DID NOT HAPPEN IN SURGERY. 5 MATTA IM CANAL FINDERS ARE BROKEN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25380249 ↗MalfunctionMay 13, 2026Material Integrity Problem
IT WAS REPORTED THAT THE MATTA CANAL FINDER TIP BROKE OFF WHEN THE DOCTOR WAS TRYING TO USE IT FOR THE FEMORAL CANAL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25163387 ↗MalfunctionMay 6, 2026Material Integrity Problem
IT WAS REPORTED THAT TIP OF THE MATTA CANAL FINDER SNAPPED OFF. BOTH PIECES WERE RECOVERED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25093520 ↗MalfunctionMay 6, 2026Material Integrity Problem
IT WAS REPORT THE TIP OF THE RASP BROKE INTRA OP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25093494 ↗MalfunctionMar 18, 2026Material Integrity Problem
IT WAS REPORTED THAT THE RASP TIP BROKE OFF IN FEMUR; SURGEON WAS ABLE TO EXTRACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24628763 ↗MalfunctionMar 18, 2026Material Integrity Problem
THE TIP OF THE RASP BROKE OFF WHEN IN USE ON A PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24628706 ↗MalfunctionFeb 10, 2026Material Integrity Problem
IT WAS REPORTED THAT BEFORE THEY STARTED BROACHING THE FEMUR TO GAIN ACCESS TO THE CANAL, THEY USED THE MATTA IM CANAL FINDER. IT WAS DISCOVERED THE TIP OF THE RASP HAD BROKEN OFF INTO THE PATIENTS FEMORAL CANAL. THEY TRIED TO RETRIEVE IT, BUT CONTINUED TO PUSH THE PIECE FARTHER DOWN INTO THE CANAL UNTIL THE SURGEON WAS FORCED TO LEAVE IT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24303448 ↗MalfunctionApr 11, 2023Material Integrity Problem; Material Integrity Problem
DID A TOTAL HIP CASE TODAY WITH THE SURGEON AND DURING THE CASE A MATTA IM CANAL FINDER BROKE OFF IN THE PATIENTS FEMORAL CANAL. AFTER AN HOUR AND A HALF, WE GOT THE BROKEN INSTRUMENT OUT OF THE PATIENTS FEMORAL CANAL. WAS SURGERY DELAYED DUE TO THE REPORTED EVENT? YES. IF YES, NUMBER OF MINUTES: AN HOUR AND A HALF.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16713495 ↗
Other Rasp devices
- ATTUNE 2545-00-048Depuy (Ireland) · RASP22 reports
- P.F.C. 85-3927Depuy (Ireland) · 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
- Calix Spinal Implant System C003-0027Xtant Medical Holdings, Inc. · RASP1 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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