BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BUCKY DIAGNOST CS 2

    MDR report key: 273073 · Received April 3, 2000

    Report

    Report Number
    1217116-2000-00005
    Event Type
    Malfunction
    Date Received
    April 3, 2000
    Date of Event
    March 2, 2000
    Report Date
    March 2, 2000
    Manufacturer
    PHILIPS SYSTEME MEDEZIN
    Product Code
    IYB
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    REPORTEDLY, AS THE TECHNOLOGIST WAS MOVING THE TUBE CRANE THE FRONT COVER DETACHED FROM THE CRANE AND FELL STRIKING THE TECHNOLOGIST. REPORTEDLY, THE TECHNOLOGIST WAS NOT INJURED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BUCKY DIAGNOST CS 2 DIAGNOSTIC X-RAY TUBE MOUNT IYB PHILIPS SYSTEME MEDEZIN 9890-010-06521 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other