BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ULTRACISION SURG DEV, BLADES 5MM, OPEN

    MDR report key: 727292 · Received June 19, 2006

    Report

    Report Number
    1527736-2006-02760
    Event Type
    Malfunction
    Date Received
    June 19, 2006
    Date of Event
    April 10, 2006
    Report Date
    April 27, 2006
    Manufacturer
    ETHICON ENDO SURGERY, INC.(CINCINNATI)
    Product Code
    LFL
    PMA / PMN Number
    k012176
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AR, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    BASED ON ANALYSIS RESULTS, THIS COMPLAINT IS NOW DETERMINED TO BE A MDR MALFUNCTION. THE ANALYSIS RESULTS FOUND THAT THE DEVICE WAS RETURNED WITH THE BLADE SCRATCHED, GOUGED AND CRACKED. THE DEVICE WAS TESTED WITH A GENERATOR AND AN ERROR CODE 5 WAS RECEIVED. THE IDENTIFIED BLADE DAMAGE MAY HAVE OCCURRED FROM EXTERNAL CONTACT DURING PRE-OP OR GENERAL USE. IN ADDITION, MINOR BLADE DAMAGE MAY INCREASE IN SEVERITY DURING SUBSEQUENT ACTIVATIONS, AND MAY RESULT IN BLADE "LOCKOUT" LATER IN THE PROCEDURE. THEREFORE, THE INSTRUCTIONAL INSERT STATES: "SCRATCHES ON THE BLADE MAY LEAD TO PREMATURE BLADE FAILURE" AND "AVOID ACCIDENTAL CONTACT WITH OTHER INSTRUMENTS DURING USE." THE BATCH RECORD WAS REVIEWED AND NO ANOMALIES WERE NOTED DURING THE MFG PROCESS. 510(K) NUMBER IS K012176.

    Description of Event or Problem · 1

    THE SYSTEM RESPONDED WITH ERROR 5 IN THE MIDDLE OF THE CASE. THE CUSTOMER RESET THE SYSTEM AND TRIED AGAIN BUT THE ERROR 5 REOCCURRED. THE DOCTOR REPLACED THE BLADE WITH ANOTHER LIKE DEVICE TO FINISH CASE. THERE WAS NO PT CONSEQUENCE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ULTRACISION SURG DEV, BLADES 5MM, OPEN LFL LFL ETHICON ENDO SURGERY, INC.(CINCINNATI) NA Y45W6G

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN 1. GENERATOR,| 2. HAND PIECE.