BEUDAMED
    FDA Adverse Event Death Summary report: N

    HP CAREVUE 9000

    MDR report key: 314991 · Received February 5, 2001

    Report

    Report Number
    1218950-2001-00038
    Event Type
    Death
    Date Received
    February 5, 2001
    Report Date
    January 7, 2000
    Manufacturer
    AGILENT TECHNOLOGIES, INC
    Product Code
    DXJ
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED TO AGILENT TECHNOLOGIES THAT A PT EXPIRED AFTER A NURSE DOUBLE CHARTED FLUID VOLUMES FOR A PT. THIS ERROR WAS NOT NOTED FOR SEVERAL HOURS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    4431 HP CAREVUE 9000 CLINICAL INFORMATION CENTER DXJ AGILENT TECHNOLOGIES, INC M2331A NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Death