BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PARADIGM INSULIN INFUSION PUMP MMT-515RNAL

    MDR report key: 1974365 · Received January 21, 2011

    Report

    Report Number
    2032227-2011-00165
    Event Type
    Injury
    Date Received
    January 21, 2011
    Date of Event
    January 4, 2010
    Report Date
    January 4, 2011
    Manufacturer
    MEDTRONIC MINIMED
    Product Code
    LZG
    PMA / PMN Number
    K040676
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    CURRENTLY, IT IS UNK 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 CALLED FOR ASSISTANCE REWINDING THE INSULIN PUMP. THE CUSTOMER THEN STATED THAT SHE WAS EXPERIENCING LOW BLOOD GLUCOSE LEVELS, AND THE PARAMEDICS WERE CALLED. ASSISTED THE CUSTOMER WITH REWINDING THE INSULIN PUMP. NOTHING FURTHER WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PARADIGM INSULIN INFUSION PUMP MMT-515RNAL INSULIN INFUSION PUMP LZG MEDTRONIC MINIMED MMT-515RNAL

    Patients

    Seq Age Sex Outcome Treatment
    1 68 YR Required Intervention