BEUDAMED
    FDA Adverse Event Death Summary report: N

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    MDR report key: 3243818 · Received July 23, 2013

    Report

    Report Number
    3004209178-2013-96001
    Event Type
    Death
    Date Received
    July 23, 2013
    Date of Event
    March 9, 2013
    Report Date
    July 12, 2013
    Manufacturer
    MEDTRONIC PUERTO RICO OPERATIONS CO.
    Product Code
    OYC
    PMA / PMN Number
    P980022
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    PATIENT FAMILY MEMBER OR FRIEND

    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 CUSTOMER PASSED AWAY, AND HE WAS NOT WEARING THE INSULIN PUMP. THE CALLER STATED BY THE TIME HIS BROTHER WAS FOUND HIS BLOOD GLUCOSE WAS LOW. THE CALLER STATED THAT THE CUSTOMER CHOCKED ON SOMETHING, AND WHEN HE GOT TO THE HOSPITAL HE WAS STILL ALIVE, BUT HE HAD A LOT OF BRAIN DAMAGE. THE CALLER STATED THAT THE FAMILY ALREADY THREW THE INSULIN PUMP AWAY. NO FURTHER INFORMATION WAS PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    342486 PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP INSULIN INFUSION PUMP / SENSOR AUGMENTED OYC MEDTRONIC PUERTO RICO OPERATIONS CO. MMT-723NAS

    Patients

    Seq Age Sex Outcome Treatment
    1 57 YR Death