BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PUMP MMT-722NAL PRDGM INS V2.2 CL EN PR

    MDR report key: 1000452 · Received February 21, 2008

    Report

    Report Number
    2032227-2008-00371
    Event Type
    Injury
    Date Received
    February 21, 2008
    Date of Event
    February 11, 2008
    Report Date
    February 12, 2008
    Manufacturer
    MEDTRONIC MINIMED
    Product Code
    LZG
    PMA / PMN Number
    P980022
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    OTHER

    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 STATED, THAT SHE WAS HOSPITALIZED DUE TO HYPERGLYCEMIA. THE BLOOD GLUCOSE READING AT THE TIME OF HOSPITALIZATION WAS NOT REPORTED. THE CUSTOMER STATED, THAT TWO DAYS PRIOR TO THE EVENT, SHE WAS VOMITING AND TOOK OFF THE INSULIN PUMP. THE CUSTOMER STATED, THAT SHE MIGHT HAVE HAD FOOD POISONING. THE CUSTOMER STATED, THAT PRIOR TO THE EVENT, SHE STARTED USING THE INSULIN PUMP AGAIN. TROUBLESHOOTING WAS PERFORMED. THE INSULIN PUMP PASSED THE PRIME, HIGH PRESSURE AND SELF TESTS. NOTHING FURTHER WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PUMP MMT-722NAL PRDGM INS V2.2 CL EN PR INFUSION PUMP LZG MEDTRONIC MINIMED MMT-722NAL

    Patients

    Seq Age Sex Outcome Treatment
    1 YR Hospitalization