MAUDE Adverse Event Report: SYMMETRY MEDICAL MANUFACTURING, INC. MATTA IM CANAL FINDER; MANUAL SURGICAL INSTRUMENT FOR GENERAL USE

Model Number	PC-002061344
Medical Device Problem Code	Material Integrity Problem (2978)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	01/12/2026
Type of Reportable Event	Malfunction
Event or Problem Description
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.
Additional Manufacturer Narrative
Device broke during a procedure.

• Brand Name: MATTA IM CANAL FINDER
• Common Device Name: MANUAL SURGICAL INSTRUMENT FOR GENERAL USE
• Manufacturer (Section D): SYMMETRY MEDICAL MANUFACTURING, INC.; 486 west 350 north; warsaw 46582
• Manufacturer (Section G): SYMMETRY MEDICAL MANUFACTURING, INC.; 486 west 350 north; warsaw 46582
• Manufacturer Contact: melanie hollett ; 486 west 350 north; warsaw 46582 ; 5742678700
• MDR Report Key: 24303448
• Report Number: 1828464-2026-05040
• Device Sequence Number: 9471575
• Product Code: HTR
• UDI-Device Identifier: 00847538010664
• UDI-Public: 00847538010664
• Combination Product (Y/N): N
• Initial Reporter State: MO
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 02/09/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: PC-002061344
• Device Catalogue Number: 10-306-000
• Device Lot Number: NOT AVAILABLE
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 02/10/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Patient Sex: Unknown