BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    OMNIPOD INSULIN PUMP

    MDR report key: 3850711 · Received March 19, 2014

    Report

    Report Number
    3004464228-2014-00350
    Event Type
    Malfunction
    Date Received
    March 19, 2014
    Date of Event
    February 22, 2014
    Report Date
    February 22, 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 DEVICE WAS NOT RETURNED FOR EVALUATION. WE ARE UNABLE TO CONFIRM THE REPORTED NEEDLE DID NOT RETRACT, OR TO DETERMINE IF IT COULD HAVE CONTRIBUTED TO THE REPORTED HYPERGLYCEMIA. LOT QUALIFICATION RECORDS WERE REVIEWED AND THE PRODUCT LOT MET ALL ACCEPTANCE CRITERIA.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT WHEN THE POD WAS REMOVED, IT WAS NOTICED THAT THE NEEDLE HAD NEVER RETRACTED. THE CUSTOMER ALSO REPORTED THAT HE WAS BLEEDING WHEN THE POD WAS REMOVED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    164191 OMNIPOD INSULIN PUMP PUMP, INFUSION, INSULIN LZG INSULET CORPORATION 14000 L40786

    Patients

    Seq Age Sex Outcome Treatment
    1 11 YR