BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    OMNIPOD INSULIN PUMP

    MDR report key: 15538415 · Received October 4, 2022

    Report

    Report Number
    3004464228-2022-18508
    Event Type
    Malfunction
    Date Received
    October 4, 2022
    Date of Event
    September 10, 2022
    Report Date
    September 10, 2022
    Manufacturer
    INSULET CORPORATION
    Product Code
    LZG
    PMA / PMN Number
    K192659
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    OTHER
    Health Professional
    N

    Narratives

    Additional Manufacturer Narrative · 0

    ACCORDING TO THE COMPLAINANT THE DEVICE WILL NOT BE RETURNED FOR INVESTIGATION. WE ARE UNABLE TO CONFIRM THE THERMAL EVENT. LOT RELEASE RECORDS WERE REVIEWED AND THE PRODUCT LOT MET ALL ACCEPTANCE CRITERIA.

    Additional Manufacturer Narrative · 0

    CORRECTION TO D(4): CATALOG NO CHANGED FROM UNAVAILABLE TO ZXP425. CORRECTION TO G(5): PMA/510(K) # CHANGED FROM UNAVAILABLE TO K192659.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT THE POD ALARMED WHILE WEARING IT ON THE ARM BETWEEN 24 AND 36 HOURS. WHEN THE POD WAS REMOVED, THE CIRCUIT BOARD IN THE POD APPEARED TO BE "HALF BURNT," AND "BROWN/BLACK." THE PATIENT IS UNSURE HOW THIS MAY HAVE HAPPENED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2539944 OMNIPOD INSULIN PUMP PUMP, INFUSION, INSULIN LZG INSULET CORPORATION 40160 L50262

    Patients

    Seq Age Sex Outcome Treatment
    1 14 YR Female