BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    DEXCOM G7

    MDR report key: 24182554 · Received January 26, 2026

    Report

    Report Number
    MW5182840
    Event Type
    Malfunction
    Date Received
    January 26, 2026
    Date of Event
    January 20, 2026
    Report Date
    January 21, 2026
    Manufacturer
    DEXCOM, INC.
    Product Code
    QBJ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TN, US
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    DEXCOM G7 SENSOR WAS READING A BLOOD GLUCOSE OF 41MG/DL. I USED MY GLUCOMETER TO CHECK MY BLOOD SUGAR AND IT WAS 93MG/DL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    247203 DEXCOM G7 INTEGRATED CONTINUOUS GLUCOSE MONITORING SYSTEM, FACTORY CALIBRATED QBJ DEXCOM, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 53 YR Male Other ALLOPURINOL. | ATENOLOL.| BUMETADINE. | GLYMPERIDE. | LEXAPRO.| METFORMIN.| MONJAURO. | POTASSIUM.| TOUJEO.