BEUDAMED
    FDA Adverse Event Injury Summary report: N

    INSTRUMENT, MANUAL, SURGICAL, GENERAL USE

    MDR report key: 23350708 · Received October 21, 2025

    Report

    Report Number
    MW5177750
    Event Type
    Injury
    Date Received
    October 21, 2025
    Date of Event
    October 2, 2025
    Report Date
    October 16, 2025
    Manufacturer
    ARTHREX, INC.
    Product Code
    MDM
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    DISPOSABLE NITINOL NEEDLE FROM THE KNEE SCORPION DEVICE BROKE WHILE PASSING SUTURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2730413 INSTRUMENT, MANUAL, SURGICAL, GENERAL USE INSTRUMENT, MANUAL, SURGICAL, GENERAL USE MDM ARTHREX, INC. AR-1299ON 15424109

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Required Intervention