BEUDAMED
    FDA Adverse Event Summary report: N

    COLLEAGUE II - TRIPLE CHANNEL IV PUMP

    MDR report key: 432102 · Received December 6, 2002

    Report

    Report Number
    MW1026932
    Date Received
    December 6, 2002
    Date of Event
    December 4, 2002
    Report Date
    December 4, 2002
    Manufacturer
    BAXTER
    Product Code
    FRN
    Report Source
    Voluntary report
    Reporter Location
    GA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    (LEVO) NOREPINEPHRINE 4ML/HR 4.27 MCG/MIN AND (NEO) PHENYLEPHRINE 27ML/HR 90 MCG/MIN WERE INFUSING IN CHANNELS 1 AND 2 IN ORDER TO MAINTAIN BP AND MEAN ARTERIAL PRESSURE >80. 0950 IV PUMP ALARMING, LEVO AND NEO NOT INFUSING, MESSAGE ON PUMP "MULTI CHANNEL PUMP FAILURE". PUMP CHANGED TO DIFFERENT PUMP DURING THE CHANGE BP DROPPED TO 86/48, MEAN ARTERIAL PRESSURE 61. THE NEW PUMP IN PLACE NEO (PHENYLEPHRINE) INCREASED 100 MCG/MIN, LEVO (NOREPINEPHRINE) INCREASED 30 MCG/MIN INITIALLY THEN DECREASED IN 10 MINS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 COLLEAGUE II - TRIPLE CHANNEL IV PUMP MULTI CHANNEL IV INFUSION PUMP FRN BAXTER 2M815316 *

    Patients

    Seq Age Sex Outcome Treatment
    1 38 YR