BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    MDR report key: 2202539 · Received August 5, 2011

    Report

    Report Number
    2032227-2011-01964
    Event Type
    Injury
    Date Received
    August 5, 2011
    Date of Event
    July 22, 2011
    Report Date
    July 24, 2011
    Manufacturer
    MEDTRONIC MINIMED
    Product Code
    MDS
    PMA / PMN Number
    P980022
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    NURSE

    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 THAT THE CUSTOMER WAS HOSPITALIZED DUE TO DIABETIC KETOACIDOSIS, WITH A BLOOD GLUCOSE READING OF 425 MG/DL. IT WAS STATED THAT THE CANNULA WAS BENT WHEN THE INFUSION SET WAS REMOVED. TROUBLESHOOTING WAS PERFORMED. THE INSULIN PUMP PASSED THE PRIME AND HIGH PRESSURE TESTS. THE CALLER REQUESTED AN INSERTION DEVICE FOR THE CUSTOMER DUE TO BENT CANNULAS WHEN INSERTING MANUALLY. 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-722LNAP

    Patients

    Seq Age Sex Outcome Treatment
    1 17 YR Hospitalization