BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    MDR report key: 13358312 · Received January 26, 2022

    Report

    Report Number
    3013756811-2022-08692
    Event Type
    Malfunction
    Date Received
    January 26, 2022
    Date of Event
    January 5, 2022
    Report Date
    January 26, 2022
    Manufacturer
    TANDEM DIABETES CARE
    Product Code
    QFG
    UDI-DI
    00850006613779
    PMA / PMN Number
    K201214
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, 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

    REPORTEDLY, CUSTOMER RECEIVED A RESUME PUMP ALARM WHEN INSULIN DELIVERIES HAD NOT BEEN STOPPED. CUSTOMER'S BLOOD GLUCOSE LEVEL WAS 100-125 MG/DL. DURING TROUBLESHOOTING TANDEM TECHNICAL SUPPORT WAS UNABLE TO CONFIRM THE CUSTOMER'S ALLEGATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    692883 T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY ALTERNATE CONTROLLER ENABLED INFUSION PUMP QFG TANDEM DIABETES CARE 1002717 00850006613779

    Patients

    Seq Age Sex Outcome Treatment
    1 59 YR Female