BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    MDR report key: 3982236 · Received August 5, 2014

    Report

    Report Number
    3004209178-2014-90157
    Event Type
    Malfunction
    Date Received
    August 5, 2014
    Date of Event
    July 5, 2014
    Report Date
    July 5, 2014
    Manufacturer
    MEDTRONIC PUERTO RICO OPERATIONS CO.
    Product Code
    OYC
    PMA / PMN Number
    P980022
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA
    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. 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

    IT WAS REPORTED THAT THE INSULIN PUMP ALARMED BATTERY OUT LIMIT DURING NORMAL USE. THE CUSTOMER'S BLOOD GLUCOSE WAS 258 MG/DL, WHICH WAS TREATED WITH MANUAL INJECTION. THE CUSTOMER WAS ADVISED THAT THIS COULD BE CAUSED BY A LOOSE BATTERY CAP. THE CUSTOMER ALSO STATED THAT THEIR BLOOD GLUCOSE METER WAS NOT TRANSMITTING THEIR BLOOD GLUCOSE READINGS TO THE INSULIN PUMP. ASSISTANCE WAS PROVIDED AND THE CORRECT METER ID WAS PROGRAMMED INTO THE INSULIN PUMP, WHICH RESOLVED THE ISSUE. NOTHING FURTHER WAS REPORTED

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    456545 PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP INSULIN INFUSION PUMP / SENSOR AUGMENTED OYC MEDTRONIC PUERTO RICO OPERATIONS CO. MMT-723NAB

    Patients

    Seq Age Sex Outcome Treatment
    1 41 YR