BEUDAMED
    FDA Adverse Event Death Summary report: N

    G6 GLUCOSE MONITOR

    MDR report key: 24369642 · Received February 17, 2026

    Report

    Report Number
    MW5183969
    Event Type
    Death
    Date Received
    February 17, 2026
    Date of Event
    May 19, 2025
    Report Date
    February 11, 2026
    Manufacturer
    DEXCOM, INC.
    Product Code
    QBJ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    WI, US
    Reporter Occupation
    PATIENT FAMILY MEMBER OR FRIEND
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    MY DAUGHTER USED A DEXCOM G6 DIABETES MONITOR. MULTIPLE TIMES HER DEXCOM WOULDN'T WORK. SHE WOULDN'T HAVE EATEN ANYTHING AND HER MONITOR WOULD READ HIGH OR SOMETIMES SHE WOULD EAT AND HER MONITOR WOULD READ LOW. SHE BECAME A TYPE 1 DIABETIC AT AGE 19. SHE WAS NOW 51, SO SHE HAD MONITORED HER DIABETES FOR MANY YEARS. HER LAST PROBLEM WITH HER DEXCOM G6 WAS WHAT TOOK HER LIFE. SHE TALKED WITH A FRIEND THAT EVENING, SAID SHE COULDN'T GET HER MONITOR TO WORK, SO SHE WAS CHECKING IT MANUALLY. SHE WENT TO BED AND WAS FOUND DECEASED IN HER BED BECAUSE SHE DIDN'T SHOW UP FOR WORK. AN AUTOPSY WAS DONE AND HER REASON FOR DEATH WAS HER DIABETES. SHE WAS RUSHED TO HOSPITAL WITH CPR BEING DONE BUT WAS GONE. I DON'T KNOW WHAT HAPPENED TO HER DEXCOM G6. WASN'T AT HER HOUSE. CORNER SAID SHE HAD A DEXCOM G6. SHE PICK UP BY UNDERTAKER TO BE CREMATED. DON'T KNOW WHERE HER MONITOR WENT, SO I CAN'T FIND HER UDI NUMBER FROM HER DEVISE. WANTED TO REPORT THIS BUT DIDN'T KNOW WHERE TO BEGIN. DID SOME READING AND WAS TOLD TO FILL OUT THIS FORM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    422317 G6 GLUCOSE MONITOR INTEGRATED CONTINUOUS GLUCOSE MONITORING SYSTEM, FACTORY CALIBRATED QBJ DEXCOM, INC. G6

    Patients

    Seq Age Sex Outcome Treatment
    1 Female Death