BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    OMMIPOD INSULIN PUMP

    MDR report key: 3963837 · Received May 20, 2014

    Report

    Report Number
    3004464228-2014-00687
    Event Type
    Malfunction
    Date Received
    May 20, 2014
    Date of Event
    April 25, 2014
    Report Date
    April 25, 2014
    Manufacturer
    INSULET CORPORATION
    Product Code
    LZG
    PMA / PMN Number
    K122953
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE PRODUCT WAS NOT RETURNED FOR EVALUATION. WE ARE UNABLE TO CONFIRM THE REPORTED BENT CANNULA OR TO DETERMINE IF IT COULD HAVE CONTRIBUTED TO THE REPORTED HYPERGLYCEMIA. QUALIFICATION RECORDS WERE REVIEWED AND THE PRODUCT LOT MET ALL ACCEPTANCE CRITERIA.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED AT 7:30AM SHE ACTIVATED A NEW POD AND HER BLOOD GLUCOSE AND INSULIN HISTORY IS AS FOLLOWS: TIME: 2:42PM, BG (MG/DL): 315, BOLUS (U): 2.45. TIME: 4:15PM, BG (MG/DL): 364. THE POD WAS THEN DEACTIVATED AND SHE NOTICED THE CANNULA WAS BENT. SHE WAS ABLE TO ACTIVATE A NEW POD.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    298338 OMMIPOD INSULIN PUMP PUMP, INFUSION, INSULIN LZG INSULET CORPORATION 14000 L40978

    Patients

    Seq Age Sex Outcome Treatment
    1 56 YR