BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK SPIRIT

    MDR report key: 1993754 · Received January 26, 2011

    Report

    Report Number
    2183996-2011-00072
    Event Type
    Malfunction
    Date Received
    January 26, 2011
    Date of Event
    January 10, 2011
    Report Date
    January 17, 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
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    ON (B)(6) 2011, PATIENT REPORTED SHE IS NOT ABLE TO DELIVER A QUICK BOLUS WITH THE DOWN BUTTON OF THE INFUSION DEVICE. PATIENT STATED SHE NOTICED THE BUTTON DID NOT WORK WHILE ATTEMPTING TO PROGRAM A QUICK BOLUS AND THE INFUSION DEVICE WOULD NOT BEEP OR VIBRATE. PATIENT REPORTED THE BUTTON POPS BACK OUT WHEN PRESSED. NO PHYSIOLOGICAL EFFECTS WERE REPORTED. THE PATIENT 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 77 YR INSULIN| INSULIN INFUSION SET