BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK SPIRIT

    MDR report key: 2143719 · Received June 3, 2011

    Report

    Report Number
    2183996-2011-01586
    Event Type
    Malfunction
    Date Received
    June 3, 2011
    Date of Event
    May 10, 2011
    Report Date
    May 13, 2011
    Manufacturer
    ROCHE INSULIN DELIVERY SYSTEMS INC.
    Product Code
    LZG
    PMA / PMN Number
    K060876
    Removal / Correction Number
    Z-1415-2009
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    ON (B)(6) 2011, PT REPORTED THE DOWN BUTTON ON THE INFUSION DEVICE IS NOT RESPONDING WHEN SHE ATTEMPTS TO BOLUS. PT STATED THE ISSUE BEGAN A FEW DAYS AGO. PT REPORTED, SHE IS CURRENTLY USING THE STANDARD BOLUS OPTION AND REMAINS ON THE INFUSION DEVICE. PT STATED, THE BUTTON DOES NOT REMAIN FLAT. NO PHYSIOLOGICAL EFFECTS WERE REPORTED. THE PT DID NOT REQUIRE ASSISTANCE FROM A HEALTHCARE PROFESSIONAL OR SECOND PARTY TO ADDRESS THE ISSUE. PRODUCT WAS REPLACED AND REQUESTED RETURN OF THE ALLEGED PRODUCT FOR EVALUATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ACCU-CHEK SPIRIT INSULIN INFUSION PUMP LZG ROCHE INSULIN DELIVERY SYSTEMS INC. NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 53 YR INSULIN INFUSION SET| INSULIN