BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    INSULIN INFUSION PUMP

    MDR report key: 4142413 · Received October 5, 2014

    Report

    Report Number
    2032227-2014-33729
    Event Type
    Malfunction
    Date Received
    October 5, 2014
    Date of Event
    September 5, 2014
    Report Date
    September 5, 2014
    Manufacturer
    MEDTRONIC MINIMED
    Product Code
    OYC
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA
    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

    IT WAS REPORTED BY THE CUSTOMER'S GRANDMOTHER THAT THEIR INSULIN PUMP WAS ALARMING NO DELIVERY. CUSTOMER VERIFIED CONNECTION BETWEEN THE RESERVOIR AND INFUSION SET WAS SECURE. CUSTOMER STATED NOT STRAIN AND INFUSION SET IS NOT BENT OR KINKED. DURING TROUBLESHOOTING, CUSTOMER WAS ASKED TO PERFORM A FIXED PRIME OF INSULIN. CUSTOMER STATES THE INSULIN DID EXIT. NEXT, CUSTOMER WAS ASKED TO MANUAL PRIME OF INSULIN. CUSTOMER STATES THE INSULIN DID EXIT AND DEVICE DID NOT ALARM. ADVISED CUSTOMER DEVICE IS FUNCTIONING AS DESIGNED. CUSTOMER'S BLOOD GLUCOSE LEVEL WAS 340 MG/DL AT TIME OF REPORTING. NOTHING FURTHER REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    621950 INSULIN INFUSION PUMP INSULIN INFUSION PUMP / SENSOR AUGMENTED OYC MEDTRONIC MINIMED MMT-XXX

    Patients

    Seq Age Sex Outcome Treatment
    1 9 YR