BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    MDR report key: 13284521 · Received January 18, 2022

    Report

    Report Number
    3013756811-2022-04926
    Event Type
    Malfunction
    Date Received
    January 18, 2022
    Date of Event
    December 31, 2021
    Report Date
    January 18, 2022
    Manufacturer
    TANDEM DIABETES CARE
    Product Code
    QFG
    UDI-DI
    00850006613779
    PMA / PMN Number
    K201214
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OK, 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.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT RESISTANCE WAS FELT WHEN FILLING MULTIPLE CARTRIDGES DURING THE LOAD SEQUENCE. CUSTOMER CHANGED MULTIPLE CARTRIDGES AND MULTIPLE SYRINGE NEEDLES TO RESOLVE THE ISSUE. CUSTOMER¿S BLOOD GLUCOSE WAS 150-192 MG/DL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    217108 T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY ALTERNATE CONTROLLER ENABLED INFUSION PUMP QFG TANDEM DIABETES CARE 1002717 W0181846 00850006613779

    Patients

    Seq Age Sex Outcome Treatment
    1 69 YR Female