BEUDAMED
    FDA Adverse Event Other Summary report: N

    CURLIN 6000 INFUSION PUMP

    MDR report key: 6145085 · Received December 1, 2016

    Report

    Report Number
    MW5066518
    Event Type
    Other
    Date Received
    December 1, 2016
    Date of Event
    September 9, 2016
    Report Date
    December 1, 2016
    Manufacturer
    MOOG
    Product Code
    FRN
    Report Source
    Voluntary report
    Reporter Location
    MI, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    PATIENT RECEIVING HYDRATION THERAPY AT HOME. THE PUMP EATING BATTERIES, SCREEN IS BLANK WHEN ALARM GOES OFF. PATIENT COULD NOT RESTART THE PUMP. THIS CAUSED A SEVERAL HOUR DELAY IN THERAPY AS NEW DEVICE HAD TO BE DELIVERED TO THE PATIENT'S HOME.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    790974 CURLIN 6000 INFUSION PUMP INFUSION PUMP FRN MOOG 6000 CMS

    Patients

    Seq Age Sex Outcome Treatment
    1 55 YR