BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NEURON DELIVERY CATHETER 070

    MDR report key: 1642414 · Received March 16, 2010

    Report

    Report Number
    3005168196-2010-00409
    Event Type
    Malfunction
    Date Received
    March 16, 2010
    Date of Event
    November 13, 2009
    Report Date
    November 13, 2009
    Manufacturer
    PENUMBRA, INC.
    Product Code
    DQY
    PMA / PMN Number
    K082290
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    THIS MDR IS BEING FILED AS PART OF THE REMEDIATION ACTION TAKEN AS PER PENUMBRA FEBRUARY 2010 UPDATE TO THE FDA WARNING LETTER DATED DECEMBER 31, 2009. A REVIEW OF THE DEVICE HISTORY RECORD (DHR) WAS COMPLETED ON PART # 2314-04 (LOT # L15780). ALL APPROPRIATE INSPECTIONS WERE COMPLETED PER PROCESS MONITORING REQUIREMENTS OR 100% INSPECTIONS WHERE REQUIRED. THE LOT HAS PASSED ALL DIMENSIONAL MEASUREMENTS PER SPECIFICATION. IN ADDITION, ALL DESTRUCTIVE TESTING WAS COMPLETED PER REQUIRED PROCESS MONITORING REQUIREMENTS AND RESULTS MET SPECIFICATION. THIS LOT WAS ASSOCIATED WITH (B)(4). THIS NCR WAS DUE TO A WIRE TRIMMING ISSUE AT THE PROXIMAL END OF THE CATHETER AND WAS FOUND BEFORE HUBBING. THE LOT WAS REPROCESSED AND UNITS THAT PASSED INSPECTION WERE ACCEPTED. THIS NCR IS NOT RELATED TO THIS INCIDENT. THE PARTS RELEASED IN THIS LOT MET PROCESS REQUIREMENT.

    Description of Event or Problem · 1

    NEURON ARRIVED WITH DAMAGED MP (EXPOSED TIP). PRODUCT WAS NOT USED, AND ANOTHER NEURON COMPLETED THE CASE. IT CAUSED NO DELAY TO TREATMENT. THE PRODUCT WAS DISPOSED OF.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NEURON DELIVERY CATHETER 070 PERCUTANEOUS CATHETER DQY PENUMBRA, INC. F15780

    Patients

    Seq Age Sex Outcome Treatment
    1