BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NASOGASTRIC FEED TUBE W/ENFIT

    MDR report key: 21197270 · Received January 21, 2025

    Report

    Report Number
    MW5164933
    Event Type
    Malfunction
    Date Received
    January 21, 2025
    Date of Event
    December 22, 2024
    Report Date
    January 14, 2025
    Manufacturer
    CARDINAL HEALTH 22, LLC.
    Product Code
    KNT
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    NURSE
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    AFTER PLACEMENT OF NGT (NASOGASTRIC TUBE), THE TUBE STARTED LEAKING WHERE THE PURPLE ACCESS PORT AND TUBE CONNECT; IT HAD TO BE REMOVED AND ANOTHER NGT WAS PLACED; UNFORTUNATELY, CAREGIVERS DID NOT SAVE ALL THE PACKAGING SO I DO NOT HAVE THE LOT OR SERIAL NUMBER; THESE TUBES ARE SUPPLIED TO US FROM BOTH CARDINAL HEALTH AND MEDLINE, UNABLE TO TELL WHERE THIS NGT WAS SUPPLIED FROM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    742612 NASOGASTRIC FEED TUBE W/ENFIT TUBES, GASTROINTESTINAL (AND ACCESSORIES) KNT CARDINAL HEALTH 22, LLC. 8884721088E

    Patients

    Seq Age Sex Outcome Treatment
    1 70 YR Male