BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNK

    MDR report key: 2894653 · Received October 4, 2007

    Report

    Report Number
    2894653
    Event Type
    Injury
    Date Received
    October 4, 2007
    Date of Event
    July 25, 2007
    Report Date
    September 17, 2007
    Manufacturer
    UNK
    Product Code
    HWC
    Report Source
    User Facility report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    SCREW REMOVAL, TRIMMIT SCREW (ARTHREX).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UNK UNK HWC UNK UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 18 YR Hospitalization| R