BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNK

    MDR report key: 2946031 · Received February 1, 2013

    Report

    Report Number
    2946031
    Event Type
    Injury
    Date Received
    February 1, 2013
    Manufacturer
    UNK
    Product Code
    UNK
    Report Source
    User Facility report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    REMOVAL OF ONE SCREW.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    45299 UNK UNK UNK UNK UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 68 YR Hospitalization