BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PROGRASP FORCEPS INSTRUMENT

    MDR report key: 2878061 · Received December 18, 2012

    Report

    Report Number
    2955842-2012-01342
    Event Type
    Malfunction
    Date Received
    December 18, 2012
    Date of Event
    August 22, 2012
    Report Date
    September 8, 2012
    Manufacturer
    INTUITIVE SURGICAL,INC.
    Product Code
    NAY
    PMA / PMN Number
    K050369
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4)

    Additional Manufacturer Narrative · 1

    ENGINEERING EVALUATION OF THE RETURNED INSTRUMENT FOUND THAT THE DISTAL END OF THE MAIN TUBE HAS VARIOUS SCRATCH MARKS WITH LIGHT MATERIAL REMOVAL. THE SCRATCHES ARE .070 - .160 IN LENGTH AND NOT ALIGNED WITH THE TUBE AXIS. THE HOUSING HAS ONE REAR SNAP TAB AND ADJACENT LOCATING PIN COMPLETELY BROKEN OFF. THE REAR CORNER OF THE HOUSING CAN BE LIFTED UP SLIGHTLY DUE TO THE DAMAGE. ENGINEERING CONCLUDED THAT THE DAMAGE IS LIKELY DUE TO MISHANDLING/MISUSE. NO OTHER DAMAGE WAS FOUND. THE INSTRUMENTS AND ACCESSORIES USER MANUAL SPECIFICALLY STATES: GENERAL PRECAUTIONS AND WARNINGS,, O HANDLE INSTRUMENTS WITH CARE. AVOID MECHANICAL SHOCK OR STRESS THAT CAN CAUSE DAMAGE TO THE INSTRUMENTS. O DO NOT USE AN INSTRUMENT TO CLEAN DEBRIS FROM ANOTHER INSTRUMENT INTRAOPERATIVELY. THIS MAY RESULT IN DAMAGE TO THE INSTRUMENTS OR OTHER UNINTENDED CONSEQUENCES, SUCH AS DISCONNECTION OF THE INSTRUMENT TIP. THE FAILURE ANALYSIS FINDINGS DO NOT CONSTITUTE A MDR REPORTABLE EVENT; HOWEVER; THE DAMAGE TO THE INSTRUMENT'S MAIN TUBE, COULD LIKELY CAUSE OR CONTRIBUTE TO AN ADVERSE EVENT IF THE MALFUNCTION WERE TO RECUR.

    Description of Event or Problem · 1

    THE PROGRASP FORCEPS INSTRUMENT WAS RETURNED BY THE SITE WITHOUT A REPORTED DEFECT. LATE SUBMISSION OF THIS MEDWATCH REPORT IS DUE TO A REPORTING OVERSIGHT BY THE RESPONSIBLE COMPLAINT HANDLER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PROGRASP FORCEPS INSTRUMENT ENDOSCOPIC INSTRUMENT NAY INTUITIVE SURGICAL,INC. 420093-08 M10110216 824

    Patients

    Seq Age Sex Outcome Treatment
    1 DA VINCI S SURG SYSTEM AND ACCESSORIES.