BEUDAMED
    FDA Adverse Event Injury Summary report: N

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

    MDR report key: 1791775 · Received August 4, 2010

    Report

    Report Number
    3004209178-2010-82352
    Event Type
    Injury
    Date Received
    August 4, 2010
    Date of Event
    July 12, 2010
    Report Date
    July 14, 2010
    Manufacturer
    MEDTRONIC PUERTO RICO OPERATIONS MED-REL
    Product Code
    LZG
    PMA / PMN Number
    P980022
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, 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 REPORTED BEING HOSPITALIZED FOR HIGH BLOOD GLUCOSE OF 575 MG/DL AND HIGH POTASSIUM LEVELS. THE CUSTOMER STATED THAT A WEEK BEFORE HER HOSPITALIZATION HAD A PROCEDURE FOR LIVER CANCER AND SHE WAS ON STEROIDS. THE CUSTOMER ALSO STATED THAT SHE WAS THROWING UP PRIOR TO HER ADMISSION. TROUBLESHOOTING WAS PERFORMED. THE BASALS AND BOLUSES WERE ADDING PROPERLY IN THE DAILY TOTALS. RAN A HIGH PRESSURE TEST AND PASSED. NO FURTHER INFORMATION WAS PROVIDED

    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 PUERTO RICO OPERATIONS MED-REL MMT-722NAL

    Patients

    Seq Age Sex Outcome Treatment
    1 69 YR Hospitalization