BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FREESTYLE LIBRE 3 PLUS

    MDR report key: 25247196 · Received May 21, 2026

    Report

    Report Number
    2954323-2026-87171
    Event Type
    Malfunction
    Date Received
    May 21, 2026
    Date of Event
    April 25, 2026
    Report Date
    May 21, 2026
    Manufacturer
    ABBOTT DIABETES CARE INC
    Product Code
    QBJ
    UDI-DI
    00357599844004
    PMA / PMN Number
    K223435
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    003

    Narratives

    Additional Manufacturer Narrative · 0

    THE PRODUCT HAS BEEN REQUESTED BACK FOR INVESTIGATION. A FOLLOW-UP REPORT WILL BE SUBMITTED UPON COMPLETION OF INVESTIGATION ACTIVITIES OR IF ADDITIONAL INFORMATION IS OBTAINED. ALL PERTINENT INFORMATION AVAILABLE TO ABBOTT DIABETES CARE HAS BEEN SUBMITTED.

    Description of Event or Problem · 0

    A CUSTOMER REPORTED RECEIVING ERRONEOUS GLUCOSE RESULTS FROM AN ABBOTT DIABETES CARE DEVICE. THE CUSTOMER RECEIVED SENSOR SCAN RESULTS OF 50, 58 MG/DL COMPARED TO READINGS OF 180, 191 MG/DL RESPECTIVELY OBTAINED ON A METER AND THE RESULTS, WHEN PLOTTED ON A PARKES ERROR GRID, FALL INTO THE C ZONE, SHOWING THE DIFFERENCE IN VALUES TO BE CLINICALLY SIGNIFICANT. THE LENGTH OF SENSOR WEAR WAS 9 DAYS. THERE WAS NO REPORT OF DEATH, SERIOUS INJURY, OR MISTREATMENT ASSOCIATED WITH THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    453773 FREESTYLE LIBRE 3 PLUS CONTINUOUS GLUCOSE MONITORING SYSTEM QBJ ABBOTT DIABETES CARE INC 78768-01 00357599844004

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown