BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PUMP MMT-715NAL PRDGM INS V2.1 CL EN

    MDR report key: 2760064 · Received May 4, 2007

    Report

    Report Number
    3004209178-2007-04695
    Event Type
    Injury
    Date Received
    May 4, 2007
    Date of Event
    April 26, 2007
    Report Date
    April 26, 2007
    Manufacturer
    MEDTRONIC PUERTO RICO OPERATIONS MED-REL
    Product Code
    LZG
    PMA / PMN Number
    K040676
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    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 STATED SHE WAS HOSPITALIZED FOR LOW BLOOD GLUCOSE LEVELS. THE CUSTOMER ALSO STATED THAT THE PARAMEDICS WERE CALLED TO HIS HOME ON TWO OTHER OCCASIONS. TROUBLESHOOTING WAS PERFORMED AND THE INSULIN PUMP PASSED THE REQUIRED TESTS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PUMP MMT-715NAL PRDGM INS V2.1 CL EN INFUSION PUMP LZG MEDTRONIC PUERTO RICO OPERATIONS MED-REL MMT-715NAL

    Patients

    Seq Age Sex Outcome Treatment
    1 29 YR Hospitalization