BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NUTRAGLIDE NASAL FEEDING TUBE

    MDR report key: 22149008 · Received June 5, 2025

    Report

    Report Number
    22149008
    Event Type
    Injury
    Date Received
    June 5, 2025
    Date of Event
    May 25, 2025
    Report Date
    June 1, 2025
    Manufacturer
    APPLIED MEDICAL TECHNOLOGY, INC.
    Product Code
    KNT
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    MA
    Reporter Occupation
    003

    Narratives

    Description of Event or Problem · 0

    5 FRENCH 90CM NUTRAGLIDE NJT [NASOJEJUNAL TUBE] PLACED ON [REDACTED] FOR NUTRITION. THE PLACEMENT OF THIS TUBE WAS CONFIRMED BY X-RAY AND INSERTION WAS DONE PER HOSPITAL POLICY. ON [REDACTED], ABOUT THREE DAYS LATER, ABDOMINAL ULTRASOUND IDENTIFIED FREE FLUID NOTED IN ABDOMEN, GIVEN HCT [HEMATOCRIT] DROP, CONCERN FOR HEMOPERITONEUM. PATIENT TRANSFERRED EMERGENTLY TO ICU [INTENSIVE CARE UNIT], INTUBATED AND GEN SURGERY EXPLORATORY LAP IDENTIFIED FEEDS PRESENT IN INTRA-ABDOMINAL SPACE AND NJT FOUND TO HAVE GONE THROUGH INTESTINAL WALL ABOUT 1 CM AT THE D2-D3 JUNCTION RIGHT AS THE DUODENUM MAKES ITS TURN. INTESTINES ALL LOOKED HEALTHY, AND NO BOWEL HAD TO BE RESECTED. HOLE WAS SEWN SHUT AND ABDOMEN CLOSED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    77357 NUTRAGLIDE NASAL FEEDING TUBE TUBES, GASTROINTESTINAL (AND ACCESSORIES) KNT APPLIED MEDICAL TECHNOLOGY, INC. ENFT-05090-I 241108-207

    Patients

    Seq Age Sex Outcome Treatment
    1 28 DA Male Required Intervention| O