BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HEWLETT PACKARD

    MDR report key: 303305 · Received November 2, 2000

    Report

    Report Number
    MW1020332
    Event Type
    Injury
    Date Received
    November 2, 2000
    Date of Event
    October 22, 2000
    Report Date
    November 2, 2000
    Manufacturer
    AGILENT TECHNOLOGIES
    Product Code
    LDD
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    DURING RESUSCITATION EFFORTS THE DEFIBRILLATOR WOULD NOT HOLD A CHARGE. WHEN NOT PLUGGED INTO WALL OUTLET. PRELIMINARY INVESTIGATION INDICATES A BAD BATTERY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HEWLETT PACKARD DEFIBRILLATOR/MONITOR LDD AGILENT TECHNOLOGIES 78671A *
    2 HEWLETT PACKARD CHARGER BASE LDD AGILENT TECHNOLOGIES * *

    Patients

    Seq Age Sex Outcome Treatment
    1 48 YR Life Threatening