BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MEDTRONIC XOMED

    MDR report key: 1028494 · Received April 4, 2008

    Report

    Report Number
    MW5006230
    Event Type
    Malfunction
    Date Received
    April 4, 2008
    Date of Event
    April 9, 2008
    Manufacturer
    MEDTRONIC XOMED
    Product Code
    GBX
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OK, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    FLUID FLOW IS RESTRICTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MEDTRONIC XOMED IRRIGATOR TUBING GBX MEDTRONIC XOMED 51501900

    Patients

    Seq Age Sex Outcome Treatment
    1