BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    MDR report key: 3842352 · Received June 1, 2014

    Report

    Report Number
    2032227-2014-02644
    Event Type
    Malfunction
    Date Received
    June 1, 2014
    Date of Event
    May 7, 2014
    Report Date
    May 7, 2014
    Manufacturer
    MEDTRONIC MINIMED
    Product Code
    OYC
    PMA / PMN Number
    P980022
    Product Problem
    Yes
    Report Source
    Manufacturer report
    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'S MOTHER REPORTED THAT THE INSULIN PUMP WAS NOT DELIVERING INSULIN PROPERLY AND GOING THROUGH A LOT OF BATTERIES. BLOOD GLUCOSE WAS 456 MG/DL AT THE TIME OF CALL. CUSTOMER HAS BEEN EXPERIENCING HIGH BLOOD GLUCOSE AND HAS CONTACTED HER PHYSICIAN. SHE HAS BEEN USING MANUAL INJECTIONS. TROUBLE SHOOTING WAS PERFORMED AND FOUND THAT THE DRIVE SUPPORT CAP WAS LOOSE. THE INSULIN PUNP WILL BE REPLACED. NO OTHER INFORMATION REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    320672 PARADIGM REAL-TIME INSULIN INFUSION PUMP INSULIN INFUSION PUMP / SENSOR AUGMENTED OYC MEDTRONIC MINIMED MMT-722LNAP

    Patients

    Seq Age Sex Outcome Treatment
    1 16 YR