BEUDAMED
    FDA Adverse Event Death Summary report: N

    HEWLETT PACKARD

    MDR report key: 159676 · Received March 26, 1998

    Report

    Report Number
    159676
    Event Type
    Death
    Date Received
    March 26, 1998
    Date of Event
    March 18, 1998
    Report Date
    March 25, 1998
    Manufacturer
    HEWLETT PACKARD MED, INC.
    Product Code
    MHX
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    IN, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    O3/17/98 PT HAD BEEN HAVING ARRHYTHMIAS ALL NIGHT. AT APPROXIMATELY 6:30 A.M., PT WAS FOUND ASYSTOLE. H.P. MONITOR HAD FAILED TO ALARM BOTH AT BEDSIDE AND AT CENTRAL STATION. ALARMS WERE FOUND TO BE TURNED OFF AFTER CODE. PT WAS DISCHARGED FROM MONITOR BEFORE BIOMED COULD DETERMINE STATUS OF ALARMS PRIOR TO CODE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HEWLETT PACKARD CARDIAC MONITOR MHX HEWLETT PACKARD MED, INC. M1092 *

    Patients

    Seq Age Sex Outcome Treatment
    1 63 YR Death