BEUDAMED
    FDA Adverse Event Summary report: N

    VERTEX PLUS MANUAL EXCHANGER

    MDR report key: 482993 · Received September 5, 2003

    Report

    Report Number
    2916556-2003-00013
    Date Received
    September 5, 2003
    Date of Event
    May 7, 2003
    Report Date
    September 4, 2003
    Manufacturer
    ADAC LABORATORIES
    Product Code
    KPS
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    DURING DETECTOR SET-UP THE TECHNOLOGIST NOTICED THE DETECTOR DRIFTING TOWARDS THE PATIENT. THERE WAS NO INJURY AT THE TIME OF THE EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VERTEX PLUS MANUAL EXCHANGER NUCLEAR MEDICINE EQUIPMENT KPS ADAC LABORATORIES 2149-3001A NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN