BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NG TUBE

    MDR report key: 4182098 · Received October 13, 2014

    Report

    Report Number
    MW5038637
    Event Type
    Injury
    Date Received
    October 13, 2014
    Date of Event
    August 20, 2014
    Report Date
    October 13, 2014
    Product Code
    KNT
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    WA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    GUIDEWIRE COULD NOT BE REMOVED AFTER PLACEMENT INTO THE PT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    645901 NG TUBE KNT 415581164X

    Patients

    Seq Age Sex Outcome Treatment
    1 52 YR Required Intervention