BEUDAMED
    FDA Adverse Event Death Summary report: N

    CODE MASTER XL+

    MDR report key: 40315 · Received September 26, 1996

    Report

    Report Number
    3017388-1996-00040
    Event Type
    Death
    Date Received
    September 26, 1996
    Date of Event
    August 27, 1996
    Report Date
    September 26, 1996
    Manufacturer
    HEWLETT PACKARD CO
    Product Code
    LDD
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    ID, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    "THE DEFIB PADS TORE AND THIS HAPPENED TO THREE DIFFERENT PADS DURING A CODE".

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CODE MASTER XL+ DEFIBRILLATOR LDD HEWLETT PACKARD CO M1722B NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Death