BEUDAMED
    FDA Adverse Event Other Summary report: N

    ZOLL MEDICAL CORPORATION

    MDR report key: 829864 · Received March 16, 2007

    Report

    Report Number
    MW1042264
    Event Type
    Other
    Date Received
    March 16, 2007
    Date of Event
    February 8, 2007
    Report Date
    March 5, 2007
    Manufacturer
    *
    Product Code
    MKJ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    FOUND UNIT WITH AC CHARGE LIGHT ON AND POWER SWITCH IN MONITOR POSITION WITH NO DISPLAY. TURNED UNIT TO DEFIB POSITION AND STILL NO DISPLAY. TURNED UNIT OFF AND REMOVED BATTERY. RE-INSTALLED BATTERY PACK AND STILL NO DISPLAY. WAS ABLE TO HEAR AUDIBLE TONE WHEN SWITCHED TO PACER MODE, BUT STILL NO DISPLAY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ZOLL MEDICAL CORPORATION DEFIBRILLATOR, MONITOR, PACEMAKER MKJ * M SERIES NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Other