BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PARADIGM INSULIN INFUSION PUMP

    MDR report key: 4112191 · Received September 23, 2014

    Report

    Report Number
    2032227-2014-27591
    Event Type
    Malfunction
    Date Received
    September 23, 2014
    Date of Event
    August 23, 2014
    Report Date
    July 10, 2018
    Manufacturer
    MEDTRONIC MINIMED
    Product Code
    LZG
    PMA / PMN Number
    K031390
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CH
    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. (B)(4).

    Additional Manufacturer Narrative · 1

    BLANK DISPLAY DUE TO MISSING BATTERY TUBE SPRING. UNABLE TO CONFIRM BUTTON ERROR ALARM OR PERFORM THE OPERATING CURRENTS MEASUREMENT, SELF TEST AND DISPLACEMENT TEST DUE TO BLANK DISPLAY ANOMALY. DEVICE HAD CORRODED KEYPAD TRACES AND CORRODED BATTERY TUBE.

    Description of Event or Problem · 1

    CUSTOMER REPORTED THAT THE INSULIN PUMP WAS RETURNING MULTIPLE BUTTON ERROR ALARMS. BLOOD GLUCOSE LEVEL WAS NOT PROVIDED. NO FURTHER INFORMATION WAS PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    592202 PARADIGM INSULIN INFUSION PUMP INSULIN INFUSION PUMP LZG MEDTRONIC MINIMED MMT-712WWL

    Patients

    Seq Age Sex Outcome Treatment
    1