BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SENSOR ENLITE

    MDR report key: 4141893 · Received October 4, 2014

    Report

    Report Number
    2032227-2014-33634
    Event Type
    Malfunction
    Date Received
    October 4, 2014
    Date of Event
    September 4, 2014
    Report Date
    September 4, 2014
    Manufacturer
    MEDTRONIC MINIMED
    Product Code
    OZO
    PMA / PMN Number
    120010
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IA
    Reporter Occupation
    PATIENT

    Narratives

    Additional Manufacturer Narrative · 1

    CURRENTLY IT IS UNKNOWN WHETHER OR NOT THE DEVICE MAY HAVE CAUSED OR CONTRIBUTED TO THE EVENT AS NO PRODUCT HAS BEEN RETURNED. THE DEVICE WILL BE RETURNED FOR ANALYSIS AND FURTHER INFORMATION WILL FOLLOW ONCE THE ANALYSIS HAS BEEN COMPLETED. NO CONCLUSION CAN BE DRAWN AT THIS TIME.

    Additional Manufacturer Narrative · 1

    ONE OPENED AND USED SENSOR WAS INSPECTED AND A BICARBONATE BUFFER TEST WAS PERFORMED. THE SENSOR FAILED PER SPECIFICATION DUE TO LOW READINGS. THE SENSOR CANNULA WAS FOUND BENT. IT COULD NOT BE CONFIRMED THAT THE SENSOR WAS RECEIVED IN SAID CONDITION DUE TO THE SENSOR BEING RETURNED OPENED AND USED.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT SHE HAD A LOW BLOOD GLUCOSE OF 47 MG/DL, WHICH SHE TREATED WITH FOOD. SHE STATED IT WAS PAST THE TIME SHE WAS SUPPOSED EAT. NOTHING FURTHER WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    621510 SENSOR ENLITE OZO OZO MEDTRONIC MINIMED MMT-7008A HG068KL

    Patients

    Seq Age Sex Outcome Treatment
    1 25 YR