BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CURLIN 6000

    MDR report key: 1892897 · Received November 1, 2010

    Report

    Report Number
    MW5018030
    Event Type
    Malfunction
    Date Received
    November 1, 2010
    Date of Event
    September 30, 2010
    Report Date
    November 1, 2010
    Manufacturer
    MOOG
    Product Code
    FRN
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MN, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    PUMP ALARMING AIR IN LINE WHEN NO AIR PRESENT IN THE TUBING. REPLACED TUBING AND PUMP STILL ALARMING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CURLIN 6000 CURLIN 6000 FRN MOOG 6000

    Patients

    Seq Age Sex Outcome Treatment
    1 65 YR