BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TEE PROBE

    MDR report key: 24031460 · Received January 12, 2026

    Report

    Report Number
    24031460
    Event Type
    Malfunction
    Date Received
    January 12, 2026
    Date of Event
    November 13, 2025
    Report Date
    December 26, 2025
    Manufacturer
    PHILIPS ULTRASOUND LLC
    Product Code
    ITX
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    NJ
    Reporter Occupation
    RISK MANAGER
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    THE ECHOCARDIOGRAM MACHINE LOST VISUALIZATION OF IMAGES THAT HAD BEEN COMING FROM THE TRANSESOPHAGEAL (TEE) PROBE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    93472 TEE PROBE TRANSDUCER, ULTRASONIC, DIAGNOSTIC ITX PHILIPS ULTRASOUND LLC

    Patients

    Seq Age Sex Outcome Treatment
    1 55 YR Male