BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NEXXIS

    MDR report key: 24698366 · Received March 26, 2026

    Report

    Report Number
    24698366
    Event Type
    Malfunction
    Date Received
    March 26, 2026
    Date of Event
    February 23, 2026
    Report Date
    March 3, 2026
    Manufacturer
    BARCO N.V.
    Product Code
    DXJ
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MN
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    DURING ENDOSCOPY PROCEDURE THIS VIDEO ROUTING DEVICE THAT ROUTES 1 OF THE VIDEO FEEDS FROM THE BACK OF THE STRYKER CAMERA BOX HAD FAILED CUTTING THE VIDEO FEED IN AND OUT INTERMITTENTLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    757659 NEXXIS DISPLAY, CATHODE-RAY TUBE, MEDICAL DXJ BARCO N.V. MNA-440

    Patients

    Seq Age Sex Outcome Treatment
    1 70 YR Male Other