MAUDE Adverse Event Report: SYMMETRY SURGICAL INC. VERITY¿ HOOK, NERVE, 3.0 MM BALL TIP; NERVE HOOK

Model Number	80-1531
Medical Device Problem Code	Break (1069)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	10/17/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The device is not available for evaluation, and the reporter was anonymous.The investigation is ongoing.Once we have additional relevant information, it will be submitted in a supplemental report.
Event or Problem Description
Complainant alleges "the tip of a micro "l" hook instrument broke during the procedure.A magnet just used to try to find it in the patient.Rolling magnets were used to search the floor and back table.All sponges and laps were searched.Drapes were searched after taken off patient as well.Machine and he said that was not an option.".
Additional Manufacturer Narrative
The device was not available for evaluation, and the reporter was anonymous.The complaint could not be confirmed and no root cause could be determined.If we get additional relevant information it will be submitted in a supplemental report.

• Brand Name: VERITY¿ HOOK, NERVE, 3.0 MM BALL TIP
• Common Device Name: NERVE HOOK
• Manufacturer (Section D): SYMMETRY SURGICAL INC.; 3034 owen drive; antioch TN 37013
• Manufacturer Contact: terry hall ; 3034 owen drive; antioch, TN 37013 ; 6166987100
• MDR Report Key: 23908466
• Report Number: 3007208013-2025-00070
• Device Sequence Number: 13034852
• Product Code: GDG
• UDI-Device Identifier: 00887482031070
• UDI-Public: 00887482031070
• Combination Product (Y/N): N
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional,User Facility
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 02/12/2026

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: 80-1531
• Device Lot Number: 93508
• 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: 12/01/2025
• Supplement Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 12/29/2025
• Supplement Report FDA Received Date: 02/12/2026
• 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: Reuse
• Patient Sequence Number: 1
• Patient Age: 57 YR
• Patient Sex: Female
• Patient Weight: 62 KG
• Patient Race: White