BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SOFTCLIX PLUS LANCET DEVICE

    MDR report key: 1070484 · Received July 7, 2008

    Report

    Report Number
    1823260-2008-05235
    Event Type
    Malfunction
    Date Received
    July 7, 2008
    Date of Event
    June 23, 2008
    Report Date
    July 7, 2008
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    FMK
    PMA / PMN Number
    EXEMPT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    LAY USER/PATIENT

    Narratives

    Description of Event or Problem · 1

    THE REPORTER STATES THAT THE LANCET DOES NOT RETRACT BACK INTO THE CAP OF THE ACCU-CHEK SOFTCLIX PLUS LANCET DEVICE BEFORE AND AFTER FIRING. NO ACTION TAKEN OR TREATMENT GIVEN BASED ON THE LANCET DEVICE ISSUE. NO ACCIDENTAL STICK OR ADVERSE EVENT REPORTED. NEW LANCET DEVICE WITH LANCETS SENT AND RETURN REQUESTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SOFTCLIX PLUS LANCET DEVICE LANCET DEVICE - FMK FMK ROCHE DIAGNOSTICS

    Patients

    Seq Age Sex Outcome Treatment
    1 44 YR SYNTHROID 130MG/DAY| LANTUS 60 UNITS/DAY| ATACAND 4MG/DAY| "TRANDOLATRIL" 4MG/DAY| LIPITOR 20MG/DAY| METFORMIN 2000MG/DAY| HUMALOG SLIDING SCALE| ACTOS 30MG/DAY