BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HOMECG+

    MDR report key: 22873951 · Received August 22, 2025

    Report

    Report Number
    3012267350-2025-00001
    Event Type
    Malfunction
    Date Received
    August 22, 2025
    Report Date
    August 22, 2025
    Manufacturer
    LOHMAN TECHNOLOGIES, LLC
    Product Code
    DXH
    UDI-DI
    00860003939734
    PMA / PMN Number
    K052767
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    THE DEVICE APPEARED TO BE OPERATING ON AN OLDER FIRMWARE VERSION WHICH WAS CAUSING ISSUES WHEN ATTEMPTING TO TAKE SCANS. THE DEVICE WAS TESTED, THEN UPDATED TO LATEST FIRMWARE AND WAS FOUND TO BE FUNCTIONAL. AFTER DELIVERY OF A NEW DEVICE WITH UPDATED FIRMWARE, THE PATIENT WAS ABLE TO SUCCESSFULLY OBTAIN SCANS.

    Description of Event or Problem · 0

    THE PATIENT REPORTS RECEIVING AN UNABLE TO ANALYZE RESULT THE MAJORITY OF THE TIME WHEN ATTEMPTING READINGS. WHEN REVIEWING DATA UPLOADED TO THE CLOUD, THERE ARE INCONSISTENCIES IN THE DATA AVAILABLE. THE PATIENT HAD NO ADVERSE EVENT OR A REACTION RESULTING FROM THIS PROBLEM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2666936 HOMECG+ TRANSMITTERS AND RECEIVERS, ELECTROCARDIOGRAPH, TELEPHONE DXH LOHMAN TECHNOLOGIES, LLC V2.0 2021 - 168283 00860003939734

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Female