BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MCKESSON NG TUBE

    MDR report key: 20631154 · Received November 6, 2024

    Report

    Report Number
    MW5162285
    Event Type
    Malfunction
    Date Received
    November 6, 2024
    Date of Event
    October 8, 2024
    Report Date
    November 5, 2024
    Manufacturer
    UKN
    Product Code
    PIF
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MA, US
    Reporter Occupation
    RISK MANAGER
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    NASOGASTRIC FEEDING TUBE GUIDEWIRE EXTREMELY DIFFICULT TO REMOVE; 3 DIFFERENT PRODUCTS TRIED BEFORE GUIDEWIRE COULD BE REMOVED WITH GREAT DIFFICULTY, CAUSING INJURY TO PROVIDER ATTEMPTING TO REMOVE IT. DOBHOFF TUBE. REFERENCE REPORT: MW5162283, MW5162284.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1875770 MCKESSON NG TUBE GASTROINTESTINAL TUBES WITH ENTERAL SPECIFIC CONNECTORS PIF UKN

    Patients

    Seq Age Sex Outcome Treatment
    1 Male Other