BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BAXTER COLLEAGUE VOLUMETRIC INFUSION PUMP

    MDR report key: 405948 · Received July 17, 2002

    Report

    Report Number
    MW1025611
    Event Type
    Malfunction
    Date Received
    July 17, 2002
    Date of Event
    July 9, 2002
    Report Date
    July 9, 2002
    Manufacturer
    BAXTER HEALTHCARE CORP, IV SYSTEM DIV
    Product Code
    FRN
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MD, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    IV PUMP IN USE IN SCN. PUMP BEGAN TO ALARM "LOW BATTERY". WHEN NURSE CHECKED PUMP IT WAS VERY HOT TO TOUCH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BAXTER COLLEAGUE VOLUMETRIC INFUSION PUMP IV PUMP FRN BAXTER HEALTHCARE CORP, IV SYSTEM DIV COLLEAGUE *

    Patients

    Seq Age Sex Outcome Treatment
    1 *