BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PROPLEGE CORONARY SINUS DEVICE

    MDR report key: 2930507 · Received January 28, 2013

    Report

    Report Number
    3008500478-2013-00373
    Event Type
    Malfunction
    Date Received
    January 28, 2013
    Date of Event
    January 9, 2013
    Report Date
    February 1, 2013
    Manufacturer
    EDWARDS LIFESCIENCES
    Product Code
    DWF
    PMA / PMN Number
    5120780
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE DEVICE WAS DISCARDED BY THE HOSPITAL. THE PRODUCT WAS NOT RETURNED AND THE ROOT CAUSE COULD NOT BE DETERMINED FOR THIS DEVICE. THEREFORE, A CAPA WAS NOT INITIATED FOR THIS EVENT. THIS INFORMATION WILL BE INCLUDED IN TRENDING AND FUTURE CAPA DETERMINATIONS.

    Additional Manufacturer Narrative · 1

    SINCE THE DEVICE WAS NOT RETURNED, ANY MANUFACTURING DEFECT WITH THE DEVICE CANNOT BE ASSESSED. HOWEVER, IT IS LIKELY THAT THE ROOT CAUSE OF THE INTRODUCER LEAKING IS RELATED TO THE ROOT CAUSE ATTRIBUTED TO SIMILAR COMPLAINTS RECEIVED FOR THE INTRORC LEAKING THAT HAVE BEEN CONFIRMED. IT IS NOT KNOWN AT THIS TIME IF THE VALVE LEAKING IS A DESIGN OR A SUPPLIER MANUFACTURING ISSUE. A CAPA HAS BEEN INITIATED IN REGARD TO THE INTRORC LEAKING COMPLAINTS. INSTRUCTIONS FOR USE WERE REVIEWED AND FOUND APPROPRIATE. THE LOT NUMBER OF THE DEVICE IN THIS CASE IS UNKNOWN; THEREFORE, AN DHR REVIEW WILL NOT BE CONDUCTED. (B)(4). A PRODUCT RECALL HAS BEEN INITIATED. TRENDS WILL CONTINUE TO BE MONITORED ON A MONTHLY BASIS AND IF FURTHER ACTION IS REQUIRED, APPROPRIATE INVESTIGATION WILL BE PERFORMED.

    Description of Event or Problem · 1

    IT WAS REPORTED BY THE SALES REP THAT THE NEW 11FR INTRODUCER OF THE PR9, CORONARY SINUS CATHETER WAS LEAKING FROM THE VALVE ONCE THE DILATOR HAD BEEN REMOVED. IT CONTINUED TO BLEED UNTIL THEY PUT A CAP ON IT. THE DID NOT RETAIN THE DEVICE FOR EVALUATION. NO PATIENT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    36926 PROPLEGE CORONARY SINUS DEVICE CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS DWF EDWARDS LIFESCIENCES PR9

    Patients

    Seq Age Sex Outcome Treatment
    1