BEUDAMED
    FDA Adverse Event Death Summary report: N

    PUMP MMT-712LNAB PRDGM INS BL EN US LN

    MDR report key: 1667351 · Received April 23, 2010

    Report

    Report Number
    2032227-2010-81019
    Event Type
    Death
    Date Received
    April 23, 2010
    Date of Event
    April 2, 2010
    Report Date
    April 9, 2010
    Manufacturer
    MEDTRONIC MINIMED
    Product Code
    LZG
    PMA / PMN Number
    K031390
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    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

    IT WAS STATED THAT THE CUSTOMER PASSED AWAY DUE TO A DIABETIC COMA. THE CUSTOMER WAS WEARING THE INSULIN PUMP AT THE TIME OF HER DEATH. UNABLE TO RETURN THE INSULIN PUMP AS IT WAS LEFT AT THE FUNERAL HOME. NOTHING FURTHER WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PUMP MMT-712LNAB PRDGM INS BL EN US LN INFUSION PUMP LZG MEDTRONIC MINIMED MMT-712LNAB

    Patients

    Seq Age Sex Outcome Treatment
    1 61 YR Death