BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    MDR report key: 4791291 · Received May 22, 2015

    Report

    Report Number
    2032227-2015-16652
    Event Type
    Malfunction
    Date Received
    May 22, 2015
    Date of Event
    December 4, 2014
    Report Date
    May 4, 2015
    Manufacturer
    MEDTRONIC MINIMED
    Product Code
    OYC
    PMA / PMN Number
    P980022
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AS
    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. THE DEVICE WILL BE RETURNED FOR ANALYSIS AND FURTHER INFORMATION WILL FOLLOW ONCE THE ANALYSIS HAS BEEN COMPLETED. NO CONCLUSION CAN BE DRAWN AT THIS TIME.

    Description of Event or Problem · 1

    CUSTOMER REPORTED VIA PHONE CALL THAT THEY HAVE BEEN EXPERIENCING ISSUES WITH THE INSULIN PUMP FOR 6 MONTHS. CUSTOMER STATED THAT THE BUTTONS ARE GETTING STUCK AND THE SCREEN WOULD KEEP SCROLLING. CUSTOMER ALSO REPORTED THAT THE INSULIN PUMP HAD CRACKS AROUND THE RESERVOIR COMPARTMENT. CUSTOMER IS ABLE TO READ THE SCREEN BUT WITH DIFFICULTY. CUSTOMER STATED THAT DAMAGE WAS JUST DUE TO WEAR AND TEAR. BLOOD GLUCOSE VALUE IS UNKNWON. CUSTOMER WAS ADVISED TO DISCONTINUE THE USE OF THE DEVICE AND REVERT TO A BACKUP PLAN. CUSTOMER WAS ADVISED THE INSULIN PUMP WOULD BE REPLACED AND AGREED TO RETURN THE PRODUCT FOR ANALYSIS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    334556 PARADIGM REAL-TIME INSULIN INFUSION PUMP INSULIN INFUSION PUMP / SENSOR AUGMENTED OYC MEDTRONIC MINIMED MMT-722LCAP

    Patients

    Seq Age Sex Outcome Treatment
    1