BEUDAMED
    FDA Adverse Event Injury Summary report: N

    VITAL PATCH

    MDR report key: 23168889 · Received September 29, 2025

    Report

    Report Number
    MW5176725
    Event Type
    Injury
    Date Received
    September 29, 2025
    Date of Event
    September 22, 2025
    Report Date
    September 24, 2025
    Manufacturer
    VITALCONNECT, INC.
    Product Code
    DRG
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NC, US
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    MEDICAL DEVICE, VITAL CONNECT BURNED MY SKIN LEAVING BURNS AND BRUISES WHERE PLACED OVER HEART.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2146276 VITAL PATCH TRANSMITTERS AND RECEIVERS, PHYSIOLOGICAL SIGNAL, RADIOFREQUENCY DRG VITALCONNECT, INC. UN 3481

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown HYDROCHLOROTHIAZIDE.| LOSARTAN.