BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ABBOTT FREE STYLE LIBRE-3 DIABETIC SENSOR

    MDR report key: 24651016 · Received March 20, 2026

    Report

    Report Number
    MW5185510
    Event Type
    Injury
    Date Received
    March 20, 2026
    Date of Event
    December 1, 2025
    Report Date
    March 13, 2026
    Manufacturer
    ABBOTT DIABETES CARE INC.
    Product Code
    QBJ
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    ABBOTT DIABETIC SENSOR FREE STYLE LIBRE 3 , IS DEFECTIVE AND DOES NOT PROVIDE ACCURATE BLOOD SUGAR READINGS AND I HAVE FALLEN, DIABETIC EMERGENCY IMPROPER READING SENT SEVERAL BACK TO ABBOTT WHO TOLD ME NOT TO FILE AND FDA COMPLAINT AS THEY WILL TAKE CARE OF THE ISSUES ALL LIES HERE ARE JUST A FEW OF THE NUMBERS THEY TOLD ME TO RETURN TO THEM. 72081-01, 72080-1, 78769-01, T60001948, T60001969 AND OTHERS. THEY ONLY SENT ME ONE DEVICE AND THAT WAS RECALLED. I HAVE SEVERAL ABBOTT LIBRE-3 FREESTYLE SENSORS ALL DEFECTIVE AND NOT GIVING ACCURATE READINGS. PT CODE: 1848. DEVICE CODE: 1535. REF REPORTS: MW5185508, MW5185509, MW5185511, MW5185512.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    717456 ABBOTT FREE STYLE LIBRE-3 DIABETIC SENSOR INTEGRATED CONTINUOUS GLUCOSE MONITORING SYSTEM, FACTORY CALIBRATED QBJ ABBOTT DIABETES CARE INC. 72081-01

    Patients

    Seq Age Sex Outcome Treatment
    1 72 YR Male Other| H| S| L