BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    MDR report key: 2133691 · Received June 9, 2011

    Report

    Report Number
    2032227-2011-01401
    Event Type
    Injury
    Date Received
    June 9, 2011
    Date of Event
    May 19, 2011
    Report Date
    May 24, 2011
    Manufacturer
    MEDTRONIC MINIMED
    Product Code
    MDS
    PMA / PMN Number
    P980022
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WI, US
    Reporter Occupation
    NOT APPLICABLE

    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

    THE CUSTOMER REPORTED THAT HE WAS HOSPITALIZED DUE TO HYPERGLYCEMIA, HYPERTENSION AND A SWOLLEN LEG. THE CUSTOMER'S BLOOD GLUCOSE READING WAS 20 MG/DL. THE CUSTOMER HAD EXPERIENCED LOW BLOOD GLUCOSE LEVELS FOR THE PAST TWO WEEKS. TROUBLESHOOTING WAS PERFORMED, AND THE CUSTOMER'S PRIMING TECHNIQUE WAS CORRECT. THE INSULIN PUMP WAS PROGRAMMED CORRECTLY. THE CUSTOMER STATED, HE WORE THE INSULIN PUMP DURING A CT AND XRAY SCAN. THE INSULIN PUMP PASSED THE DISPLACEMENT TEST. NOTHING FURTHER WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PARADIGM REAL-TIME INSULIN INFUSION PUMP INSULIN INFUSION PUMP MDS MEDTRONIC MINIMED MMT-722LNAS

    Patients

    Seq Age Sex Outcome Treatment
    1 64 YR Hospitalization