BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ARTHREX

    MDR report key: 2024038 · Received March 2, 2011

    Report

    Report Number
    2024038
    Event Type
    Malfunction
    Date Received
    March 2, 2011
    Date of Event
    February 23, 2011
    Report Date
    March 2, 2011
    Manufacturer
    ARTHREX
    Product Code
    LXH
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    CA, US

    Narratives

    Description of Event or Problem · 1

    SURGEON WAS USING A RING CURETTE DURING AN ORTHOPEDIC CASE AND THE TIP OR "RING" AREA OF THE CURETTE BROKE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ARTHREX RING CURETTE LXH ARTHREX AR-20020 00612

    Patients

    Seq Age Sex Outcome Treatment
    1 15 YR