BEUDAMED
    FDA Adverse Event Death Summary report: N

    HEWLETT PACKARD

    MDR report key: 299602 · Received October 5, 2000

    Report

    Report Number
    299602
    Event Type
    Death
    Date Received
    October 5, 2000
    Date of Event
    October 4, 2000
    Report Date
    October 5, 2000
    Manufacturer
    AGILENT TECHNOLOGIES
    Product Code
    DRT
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    KY, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    PT WAS ON CARDIAC MONITOR IN ICU. PT WAS POST-CARDIAC SURGERY. PT WAS FOUND IN ROOM BY RN UNRESPONSIVE IN FULL ARREST. THERE WERE NO ALARMS THAT ALERTED THE NURSING STAFF THAT PT WAS IN DISTRESS. IT IS UNCERTAIN AT THIS TIME IF THIS WAS USER ERROR OR MACHINE MALFUNCTION. FULL INVESTIGATION TO BE DONE ON EQUIPMENT AND CIRCUMSTANCES SURROUNDING THE EVENT; PT EXPIRED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HEWLETT PACKARD CENTRAL DISPLAY MONITOR DRT AGILENT TECHNOLOGIES 78510B *
    2 HEWLETT PACKARD MONITOR CPU DRT AGILENT TECHNOLOGIES M1046A *
    3 HEWLETT PACKARD BEDSIDE MONITOR DRT AGILENT TECHNOLOGIES M-1092A-BEDSIDE *

    Patients

    Seq Age Sex Outcome Treatment
    1 72 YR Death