BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    COLLEAGUE VOLUMETRIC INFUSION PUMP

    MDR report key: 1241632 · Received November 25, 2008

    Report

    Report Number
    6000001-2007-04199
    Event Type
    Malfunction
    Date Received
    November 25, 2008
    Date of Event
    January 1, 2007
    Report Date
    January 16, 2007
    Manufacturer
    BAXTER HEALTHCARE PTE. LTD.
    Product Code
    FRN
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TN, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    EVALUATION SUMMARY: THE CONDITION OF AIR-IN-LINE ALARMS WAS CONFIRMED. THE AIR-IN-LINE ALARMS WERE CAUSED BY THE AIR-IN-LINE SENSOR BEING OUT OF SPECIFICATION. THE AIR-IN-LINE SENSOR WAS RECALIBRATED BUT THE AIR-IN-LINE ALARMS CONTINUED. THE PUMP HEAD MODULE WHICH CONTAINS THE AIR-IN-LINE SENSOR WAS REPLACED WHICH CORRECTED THE CONDITION.

    Description of Event or Problem · 1

    THE FACILITY REPORTED AN INFUSION PUMP WITH AIR-IN-LINE ALARMS. THE EVENT WAS REPORTED TO HAVE OCCURRED DURING BIOMED TESTING. ACCORDING TO THE HOSPITAL REPRESENTATIVE, NO PATIENT INJURY OR MEDICAL INTERVENTION HAD BEEN REPORTED RELATED TO THE DEVICE. NO ADDITIONAL INFORMATION OR CONTACT WAS AVAILABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 COLLEAGUE VOLUMETRIC INFUSION PUMP INFUSION PUMP FRN BAXTER HEALTHCARE PTE. LTD. N/A NA

    Patients

    Seq Age Sex Outcome Treatment
    1