BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

    MDR report key: 9072977 · Received September 16, 2019

    Report

    Report Number
    3013756811-2019-59741
    Event Type
    Malfunction
    Date Received
    September 16, 2019
    Date of Event
    August 20, 2019
    Report Date
    September 16, 2019
    Manufacturer
    TANDEM DIABETES CARE
    Product Code
    OZO
    UDI-DI
    00853052007325
    PMA / PMN Number
    P180008
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT AN UNSPECIFIED MALFUNCTION OCCURRED. CUSTOMER'S BLOOD GLUCOSE LEVEL WAS 200-360 MG/DL. REPORTEDLY, THE CUSTOMER HAD AN ALTERNATE PUMP AVAILABLE FOR INSULIN THERAPY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    865575 T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY AUTOMATED INSULIN DOSING, THRESHOLD SUSPEND OZO TANDEM DIABETES CARE 1000096 00853052007325

    Patients

    Seq Age Sex Outcome Treatment
    1 16 YR