BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DEXCOM G7

    MDR report key: 23780774 · Received December 11, 2025

    Report

    Report Number
    MW5180377
    Event Type
    Injury
    Date Received
    December 11, 2025
    Date of Event
    August 1, 2025
    Report Date
    December 7, 2025
    Manufacturer
    DEXCOM, INC.
    Product Code
    QBJ
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OH, US
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    FIRST, I SPOKE TO MY DOCTOR IN REFERENCE TO THE PROBLEM AND HE BLEW IT OFF AND SAID YOU'RE SUFFERING FROM ANXIETY. THAT IS WHAT'S CAUSING THE PROBLEM. SO, I SWITCHED DOCTORS AND WENT TO SEE AN ENDOCRINOLOGIST AND SHE WOULDN'T DO ANYTHING IN REFERENCE TO THE PROBLEM. I CALLED THE TRIAGE NURSE AT THE VA AND THEY HAD ME TO GO TO THE NEAREST EMERGENCY ROOM FOR MY DIABETES. WELL, WHEN I GOT THERE, MY DIABETES HAD TOOK A TOLL ON MY HEART AND I HAD TO HAVE STENTS PUT IN MY HEART. I WAS ITCHING ALL OVER MY BODY ALL IN MY EYES AND THE ER DOCTOR TOLD ME WE CAN'T LET YOU GO HOME. WE'RE GOING TO HAVE TO PUT YOU IN THE HOSPITAL AND THAT HOSPITAL WAS (B)(6).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2780361 DEXCOM G7 INTEGRATED CONTINUOUS GLUCOSE MONITORING SYSTEM, FACTORY CALIBRATED QBJ DEXCOM, INC. 1725194005

    Patients

    Seq Age Sex Outcome Treatment
    1 68 YR Male Other| H INSPIRE THERAPY