BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DELTEC COZMO INSULIN PUMP

    MDR report key: 1193284 · Received October 7, 2008

    Report

    Report Number
    2183502-2008-00295
    Event Type
    Injury
    Date Received
    October 7, 2008
    Date of Event
    September 6, 2008
    Report Date
    October 6, 2008
    Manufacturer
    SMITHS MEDICAL MD (FORMERLY DELTEC, INC)
    Product Code
    LZG
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    EVAL SUMMARY: THE SUSPECT DEVICE WAS RETURNED AND EVALUATED. DELIVERY AND ACCURACY TESTS WERE PERFORMED, THE DEVICE WAS FOUND TO PASS ALL DELIVERY AND ACCURACY TESTS. NO OPERATIONAL OR FUNCTIONAL FAILURE WAS DETECTED AND THE PRODUCT WAS WITHIN SPECIFICATION.

    Description of Event or Problem · 1

    INFO WAS RECEIVED THAT REPORTED A PT WAS HOSPITALIZED IN 2008, DUE TO AN INCIDENT OF DIABETIC KETOACIDOSIS. PER THE REPORT THE PT HAD HIGH BLOOD GLUCOSE FOR GREATER THEN 24 HOURS. PRIOR TO ADMIT, THE PT HAD BLOOD GLUCOSE >500 MG/DL. UPON ADMIT THE PT HAD A BLOOD GLUCOSE OF 730 MG/DL AND WAS DIAGNOSED IN DIABETIC KETOACIDOSIS. THE PT WAS TREATED WITH IV FLUIDS AND INSULIN. THE DEVICE WILL BE RETURNED FOR EVAL; TO ENSURE THAT IT IS FUNCTIONING CORRECTLY AND DID NOT CONTRIBUTE TO THE REPORTED INCIDENCE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DELTEC COZMO INSULIN PUMP INSULIN PUMP LZG SMITHS MEDICAL MD (FORMERLY DELTEC, INC) 1800 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 Hospitalization