BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LIBRE 3 PLUS SENSOR

    MDR report key: 23863923 · Received December 22, 2025

    Report

    Report Number
    MW5180918
    Event Type
    Injury
    Date Received
    December 22, 2025
    Date of Event
    December 15, 2025
    Report Date
    December 15, 2025
    Manufacturer
    ABBOTT DIABETES CARE INC.
    Product Code
    QBJ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    REPORTING THAT I HAVE 5 UNITS THAT WAS FOUND ON THE RECALL SHEET LOT# T60003596. NEED TO KNOW WHAT'S THE NEXT STEP. (B)(6)- 940-367-0886- (B)(6) 76201 (940) 735 3119 LIBRE3 PLUS SENSOR. PT CODE: 4582. DEVICE CODE: 1420. REF REPORTS: MW5180917, MW5180919, MW5180920, MW5180921.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2695138 LIBRE 3 PLUS SENSOR INTEGRATED CONTINUOUS GLUCOSE MONITORING SYSTEM, FACTORY CALIBRATED QBJ ABBOTT DIABETES CARE INC. T60003596

    Patients

    Seq Age Sex Outcome Treatment
    1 2 MO Male Required Intervention