BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ARTHREX, INC. SCORPION NEEDLE, KNEE

    MDR report key: 18436849 · Received January 2, 2024

    Report

    Report Number
    MW5149733
    Event Type
    Malfunction
    Date Received
    January 2, 2024
    Date of Event
    December 28, 2023
    Report Date
    December 28, 2023
    Manufacturer
    ARTHREX, INC.
    Product Code
    MDM
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    DURING REPAIR LEFT KNEE ACL(ANTERIOR CRUCIATE LIGAMENT INJURY) RUPTURED MEDIAL MENISCUS TEAR, THE TIP OF THE SCORPION KNEE NEEDLE WAS NOTED TO BE MISSING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1699623 ARTHREX, INC. SCORPION NEEDLE, KNEE INSTRUMENT, MANUAL, SURGICAL, GENERAL USE MDM ARTHREX, INC. AR-1299ON 15150737

    Patients

    Seq Age Sex Outcome Treatment
    1 30 YR Unknown Other