BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    MDR report key: 18317948 · Received December 13, 2023

    Report

    Report Number
    3013756811-2023-177237
    Event Type
    Malfunction
    Date Received
    December 13, 2023
    Date of Event
    November 14, 2023
    Report Date
    December 13, 2023
    Manufacturer
    TANDEM DIABETES CARE
    Product Code
    QFG
    UDI-DI
    00850006613762
    PMA / PMN Number
    K201214
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    DE, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    NO PRODUCT WAS RETURNED FOR EVALUATION. SHOULD NEW RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. H3 OTHER TEXT : DEVICE NOT RETURNED.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT AN INTERMITTENT CARTRIDGE ALARM 0 OCCURRED WITH MULTIPLE CARTRIDGES. THE PUMP WAS RESET AND A NEW CARTRIDGE WAS LOADED TO RESOLVE THE ISSUE. CUSTOMER'S BLOOD GLUCOSE LEVEL WAS 100-269 MG/DL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1695176 T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY ALTERNATE CONTROLLER ENABLED INFUSION PUMP QFG TANDEM DIABETES CARE 1002717 00850006613762

    Patients

    Seq Age Sex Outcome Treatment
    1 39 YR Female INSULIN: NOVOLOG/NOVORAPID