BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PUMP MMT-523RNAB PRDGM INS V2.3 BL EN RC

    MDR report key: 1843483 · Received September 20, 2010

    Report

    Report Number
    2032227-2010-82703
    Event Type
    Injury
    Date Received
    September 20, 2010
    Date of Event
    August 30, 2010
    Report Date
    August 31, 2010
    Manufacturer
    MEDTRONIC MINIMED
    Product Code
    MDS
    PMA / PMN Number
    P980022
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MO, US
    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

    THE CUSTOMER REPORTED THAT THE INSULIN PUMP WAS BEEPING. THE CUSTOMER THEN STATED THAT SHE EXPERIENCED LOW BLOOD GLUCOSE LEVELS YESTERDAY AND THE PARAMEDICS WERE CALLED, BUT SHE WAS NOT ADMITTED. NOTHING FURTHER WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PUMP MMT-523RNAB PRDGM INS V2.3 BL EN RC INFUSION PUMP MDS MEDTRONIC MINIMED MMT-523RNAB

    Patients

    Seq Age Sex Outcome Treatment
    1 74 YR Required Intervention