BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    MDR report key: 13175039 · Received January 6, 2022

    Report

    Report Number
    3013756811-2022-01784
    Event Type
    Malfunction
    Date Received
    January 6, 2022
    Date of Event
    December 7, 2021
    Report Date
    January 6, 2022
    Manufacturer
    TANDEM DIABETES CARE
    Product Code
    QFG
    UDI-DI
    00853052007264
    PMA / PMN Number
    K201214
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    OTHER
    Health Professional
    N

    Narratives

    Additional Manufacturer Narrative · 0

    THE DEVICE IS EXPECTED TO BE RETURNED; HOWEVER, THE DEVICE HAS NOT YET BEEN RECEIVED. A SUPPLEMENTAL REPORT WILL BE SUBMITTED IF THE DEVICE IS RECEIVED AND EVALUATION IS PERFORMED.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT THE WAKE BUTTON WAS DELAYED IN RESPONDING TO TOUCH. CUSTOMER¿S BLOOD GLUCOSE LEVEL RANGED BETWEEN 150-166 MG/DL. REPORTEDLY THE CUSTOMER CONTINUED TO USE THE PUMP FOR INSULIN THERAPY.

    Description of Event or Problem · 0

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    666219 T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY ALTERNATE CONTROLLER ENABLED INFUSION PUMP QFG TANDEM DIABETES CARE 1002717 00853052007264

    Patients

    Seq Age Sex Outcome Treatment
    1 16 YR Female INSULIN: HUMALOGINFUSION: AUTOSOFT 30