BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TANDEM T:SLIM INSULIN DELIVERY SYSTEM

    MDR report key: 4843589 · Received June 12, 2015

    Report

    Report Number
    3007981285-2015-33680
    Event Type
    Injury
    Date Received
    June 12, 2015
    Date of Event
    May 16, 2015
    Report Date
    May 16, 2015
    Manufacturer
    TANDEM DIABETES CARE INC.
    Product Code
    LZG
    PMA / PMN Number
    K111210
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SC, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    THE DEVICE IS EXPECTED TO BE RETURNED; HOWEVER, THE DEVICE HAS NOT YET BEEN REC'D. A SUPPLEMENTAL REPORT WILL BE SUBMITTED IF THE DEVICE IS REC'D.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE CUSTOMER RECEIVED AN ALTITUDE ALARM RIGHT AFTER LOADING A NEW CARTRIDGE. PRIOR TO RECEIVING THE ALARM, THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS 600 MG/DL. THE CUSTOMER REMOVED AND REINSTALLED THE CARTRIDGE. THERE WAS TEMPORARY DELAY IN CLEARING THE ALARM AND RESUMING INSULIN DELIVERY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    383851 TANDEM T:SLIM INSULIN DELIVERY SYSTEM INSULIN PUMP LZG TANDEM DIABETES CARE INC. 004628

    Patients

    Seq Age Sex Outcome Treatment
    1 25 YR Other