BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ZOLL MEDICAL CORP.

    MDR report key: 262279 · Received February 11, 2000

    Report

    Report Number
    262279
    Event Type
    Malfunction
    Date Received
    February 11, 2000
    Date of Event
    February 4, 2000
    Report Date
    February 10, 2000
    Manufacturer
    ZOLL MEDICAL CORP.
    Product Code
    LDD
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    CA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    PT ARRESTED. CODE BLUE CALLED. PT HOOKED UP TO DEFIBRILLATOR. MACHINE TURNED 'ON'. NURSE HEARD A CLICK AND SAW A FLICK OF LIGHT ACROSS THE SCREEN AND THEN THE SCREEN WENT BLANK. NEW MONITOR USED, LOW BATTERY. BATTERY CHARGED. CODE CONTINUED. CODE ENDED AFTER 39 MINS. PT PRONOUNCED DEAD.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ZOLL MEDICAL CORP. DEFIBRILLATOR LDD ZOLL MEDICAL CORP. 101138 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 76 YR Other