BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SENSOR ENLITE

    MDR report key: 4201265 · Received October 27, 2014

    Report

    Report Number
    2032227-2014-43015
    Event Type
    Malfunction
    Date Received
    October 27, 2014
    Date of Event
    September 24, 2014
    Report Date
    September 24, 2014
    Manufacturer
    MEDTRONIC MINIMED
    Product Code
    OZO
    PMA / PMN Number
    120010
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO
    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. NO CONCLUSION CAN BE DRAWN AT THIS TIME. WE THEREFORE CONSIDER THIS REPORT COMPLETE TO THE BEST OF OUR KNOWLEDGE.

    Description of Event or Problem · 1

    CUSTOMER REPORTS THAT INSULIN PUMP FAILED. CUSTOMER STATES SHE WAS ABLE TO REPROGRAM PUMP BUT HAD PROBLEMS CONNECTING SENSOR. CUSTOMER STATES THE SENSOR AND SERTER FELL APART. CUSTOMER ALSO REPORTS BLEEDING AT SENSOR SITE. CUSTOMER'S BLOOD GLUCOSE WAS 90 MG/DL. CUSTOMER WAS ADVISED TO REPLACE SENSOR AS BLOOD ON CONNECTOR CAN DAMAGE TRANSMITTER PINS. SENSOR WILL BE REPLACED. NO FURTHER INFORMATION PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    682347 SENSOR ENLITE OZO OZO MEDTRONIC MINIMED MMT-7008A

    Patients

    Seq Age Sex Outcome Treatment
    1 57 YR