BEUDAMED
    FDA Adverse Event Other Summary report: N

    SERIES 8000 BUCKY

    MDR report key: 16969 · Received March 18, 1994

    Report

    Report Number
    2126677-1994-00001
    Event Type
    Other
    Date Received
    March 18, 1994
    Date of Event
    January 17, 1994
    Report Date
    February 8, 1994
    Manufacturer
    LIEBEL-FLARSHEIM
    Product Code
    IXJ
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    KY, US
    Reporter Occupation
    RADIOLOGIC TECHNOLOGIST

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTER TO GE THAT THE TECHNOLOGIST PULLED THE CASSETTE TRAY ALL THE WAY OUT ALLOWING IT TO FALL AND STRIKE HIS FOTT. APPARENTLY, THIS CAUSED A FRACTURE OF THE TOE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SERIES 8000 BUCKY X0RAY BUCKY IXJ LIEBEL-FLARSHEIM UNKNOWN UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Other