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

Model Number	259807013
Medical Device Problem Code	Material Integrity Problem (2978)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	02/19/2026
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that the rasp tip broke off in femur; surgeon was able to extract.

• 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 IN 46582
• Manufacturer Contact: melanie hollett ; 486 west 350 north; warsaw, IN 46582 ; 5742678700
• MDR Report Key: 24628763
• Report Number: 1828464-2026-05150
• Device Sequence Number: 18409080
• Product Code: HTR
• UDI-Device Identifier: 00847538010664
• UDI-Public: 00847538010664
• Combination Product (Y/N): N
• Initial Reporter State: IN
• 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): 03/17/2026

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: 259807013
• Device Catalogue Number: 10-306-000
• Device Lot Number: UNKNOWN
• 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: 03/18/2026
• 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