BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    DEXCOM G6 GLUCOSE PROGRAM CONTINUOUS GLUCOSE MONITORING (CGM) SYSTEM

    MDR report key: 13097242 · Received December 28, 2021

    Report

    Report Number
    3004753838-2021-434159
    Event Type
    Malfunction
    Date Received
    December 28, 2021
    Date of Event
    December 8, 2021
    Report Date
    December 28, 2021
    Manufacturer
    DEXCOM, INC.
    Product Code
    QDK
    PMA / PMN Number
    K203089
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NH, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    (B)(4).

    Description of Event or Problem · 0

    IT WAS REPORTED THAT AN INACCURACY BETWEEN THE CONTINUOUS GLUCOSE MONITOR (CGM) AND THE BLOOD GLUCOSE (BG) METER OCCURRED. THE SENSOR WAS INSERTED INTO THE ABDOMEN ON (B)(6) 2021. IT WAS INDICATED THAT THE PATIENT USED AN EXPIRED SENSOR, WHICH IS OFF-LABEL USAGE OF THE DEVICE. NO DATA WAS PROVIDED FOR EVALUATION. CONFIRMATION OF THE ALLEGATION AND A PROBABLE CAUSE COULD NOT BE DETERMINED. THE REPORTED GLUCOSE VALUES FALL WITHIN THE D ZONE OF THE PARKES ERROR GRID. NO INJURY OR MEDICAL INTERVENTION WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1992458 DEXCOM G6 GLUCOSE PROGRAM CONTINUOUS GLUCOSE MONITORING (CGM) SYSTEM CONTINUOUS GLUCOSE MONITOR QDK DEXCOM, INC. 5278611

    Patients

    Seq Age Sex Outcome Treatment
    1 73 YR Female