BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FREESTYLE LIBRE 3 PLUS

    MDR report key: 23817609 · Received December 16, 2025

    Report

    Report Number
    MW5180590
    Event Type
    Malfunction
    Date Received
    December 16, 2025
    Manufacturer
    ABBOTT DIABETES CARE INC.
    Product Code
    QBJ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    AZ, US
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    I HAVE TWO BOXES OF UNOPENED LIBRE FREESTYLE PLUS 3 GLUCOSE SENSORS THAT ARE ON A RECALL LIST SENT TO ME BY WALMART INC. LOT #: T60003596, T60003592. WHAT CAN I DO TO GET TWO REPLACEMENT SENSORS? WHAT DO I DO WITH RECALLED SENSORS? (B)(6). PATIENT CODE: 4580. DEVICE CODE: 1420. REFERENCE REPORT: MW5180591.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2182187 FREESTYLE LIBRE 3 PLUS INTEGRATED CONTINUOUS GLUCOSE MONITORING SYSTEM, FACTORY CALIBRATED QBJ ABBOTT DIABETES CARE INC. T60003592

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Female