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	09/02/2026
Type of Reportable Event	Malfunction

• 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 ; +1(574)267-8700
• MDR Report Key: 50760685
• Report Number: 1828464-2026-05652
• Device Sequence Number: 9333492
• Product Code: HTR
• UDI-Device Identifier: 00847538010664
• UDI-Public: 00847538010664
• Combination Product (Y/N): N
• Initial Reporter State: NJ
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Type of Report: Initial
• Report Date (Section B): 09/14/2026

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: SO2068086
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 09/14/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 05/15/2025
• 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