BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TANDEM T: SLIM INSULIN DELIVERY DEVICE

    MDR report key: 3922117 · Received May 30, 2014

    Report

    Report Number
    3007981285-2014-00869
    Event Type
    Malfunction
    Date Received
    May 30, 2014
    Date of Event
    April 30, 2014
    Report Date
    May 1, 2014
    Manufacturer
    TANDEM DIABETES
    Product Code
    LZG
    PMA / PMN Number
    K111210
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    DURING FURTHER TROUBLESHOOTING IT WAS IDENTIFIED LUER WAS LOOSE. CHECK THAT YOUR LUER-LOCK CONNECTION BETWEEN THE CARTRIDGE TUBING AND THE INFUSION SET TUBING IS TIGHT AND SECURE.

    Description of Event or Problem · 1

    RECEIVED INFORMATION STATING PATIENT WAS EXPERIENCING HIGH BG'S (300 MG/DL).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    320095 TANDEM T: SLIM INSULIN DELIVERY DEVICE INSULN PUMP LZG TANDEM DIABETES 004628

    Patients

    Seq Age Sex Outcome Treatment
    1 56 YR