BEUDAMED
    FDA Adverse Event Death Summary report: N

    INFUSION PUMP

    MDR report key: 17880 · Received October 26, 1994

    Report

    Report Number
    17880
    Event Type
    Death
    Date Received
    October 26, 1994
    Date of Event
    October 16, 1994
    Report Date
    October 26, 1994
    Manufacturer
    BAXTER HEALTHCARE CORP.
    Product Code
    FRN
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    NJ, US
    Reporter Occupation
    BIOMEDICAL ENGINEER

    Narratives

    Description of Event or Problem · 1

    PT ADMITTED TO ICU 10/15/94 IN ADVANCED STAGE OF LIVER AND RENAL FAILURE, PLACED IN "COMFORT CARE" (NO CODE) STATUS. A: 3.30 PM ON 10/16/74 IV 100 MG MORPHINE STARTED AT 2 CC/HR. VOLUME SET TO INFUSE 100 CC. AT 6:00 PM MORPHINE BAG FOUND TO BE EMPTY (ENTIRE 100 CC WAS INFUSED). PT EXPIRED 7:01 PM. PUMP WAS IMPOUNDED BY COUNTY MEDICAL EXAMINER AND WAS SUBSEQUENTLY SENT FOR EVALUATION. INITIAL TOXICOLOGY REPORTS INDICATED ELEVATED LEVELS OF MORPHINE IN PT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 INFUSION PUMP INFUSION PUMP FRN BAXTER HEALTHCARE CORP. 6301

    Patients

    Seq Age Sex Outcome Treatment
    1 53 YR Death