BEUDAMED
    FDA Adverse Event Other Summary report: N

    THORAVISION

    MDR report key: 527184 · Received February 17, 2004

    Report

    Report Number
    1217116-2004-00003
    Event Type
    Other
    Date Received
    February 17, 2004
    Date of Event
    January 20, 2004
    Report Date
    January 20, 2004
    Manufacturer
    PHILIPS MEDICAL SYSTEMS
    Product Code
    KPR
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    A PT WAS HAVING A CHEST X-RAY PERFORMED BY THE THORAVISION. IT WAS MOVING UPWARD WHEN IT FELL DOWNWARD ABOUT 0.3 METERS. THE PT WAS UNINJURED BUT IF THEY HAD BEEN POSITIONED DIFFERENTLY A STEEL BAR MAY HAVE STRUCK THE PT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 THORAVISION STATIONARY DIAGNOSTIC CHEST X-RAY SYSTEM KPR PHILIPS MEDICAL SYSTEMS MTD3003 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other