Device Recall MAQUET

  • Modelo / Serial
    Lot numbers: 201413, 201414, 201415, 201417, 201419 and 201422.
  • Clasificación del producto
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Distributed to FL, KS, MI and WV.
  • Descripción del producto
    MAQUET, SERVO Humidifier 163, Rx Only, Inmed Mfg. Sdn Bhd. Catalog No: XKC01-06-8125-8, Model No. 01-06-8125-8. || A heat and moisture condenser (artificial nose) is a device intended to be positioned over a tracheotomy (a surgically created opening in the throat) or tracheal tube (a tube inserted into the trachea) to warm and humidify gases breathed in by a patient.
  • Manufacturer
  • 1 Event

Fabricante

  • Dirección del fabricante
    Teleflex Medical, 4024 Stirrup Creek Dr, Durham NC 27703-9000
  • Empresa matriz del fabricante (2017)
  • Source
    USFDA

34 dispositivos con un nombre similar

Más información acerca de la data acá

  • Modelo / Serial
    Sensation 7 fr.34 cc IAB Demonstration Unit  0684-DC-0433 0684-DO-0433 0684-DC-0469 0684-DO-0469  Sensation 7 Fr. 40 cc IAB Demonstration Unit 0684-DC-0434 0684-DO-0434 0684-DC-0470 0684-DO-0470  Sesnsation Plus 7.5 Fr. 40cc IAB Demonstration Units  0684-DC-0567 0684-DO-0567 0684-DC-0568 0684-DO-0568  Sensation Plus 7.5 Fr. 50cc IAB Demonstration Units 0684-DC-0575 0684-DO-0575 0684-DC-0576 0684-DO-0576  Sensation Plus 8 Fr. 50 cc IAB Demonstration Unit 0684-DC-0272 0684-DO-0272
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution
  • Descripción del producto
    CARDIOSAVE Intra-Aortic Balloon Pump and CS300 Intra-Aortic Balloon Pump; and, non-sterile, not for human use, SENSATION and SENSATION PLUS IABC demonstration units. Part Number 0998-00-0800-xx; 0998-00-3023-xx; 0998-UC-0800-xx; 0998-UC-3023-xx || An electromechanical system used to inflate and deflate intra-aortic balloons.
  • Manufacturer
  • Modelo / Serial
    Batch Numbers: 201321, 201323, and 201324.
  • Clasificación del producto
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Distributed in the states of FL, MI, WV, and KS.
  • Descripción del producto
    MAQUET Servo Humidifier 163; Model No.: 01-06-8125-8, catalog no. XKC01-06-8125-8. || A heat and moisture condenser (artificial nose) is a device intended to be positioned over a tracheotomy (a surgically created opening in the throat) or tracheal tube (a tube inserted into the trachea) to warm and humidify gases breathed in by a patient.
  • Manufacturer
  • Modelo / Serial
    Serial Numbers:  9592 9604 9606 9608 9609 9610 9611 9612 9616 9617 9618 9619 9620 9621 9625 9626 9627 9636 9643 9645 9646 9647 9648 9649 9650 9651 9652 9653 9654 9655 9656 9657 9658 9659 9660 9661 9662 9664 9666 9667 9668 9669 9670 9671 9674 9676 9677 9678 9679 9680 9681 9682 9683 9684 9686 9687 9689 9690 9692 9697 9698 9702 9706 9708 9709 9712 9716 9718 9720 9721 9727 9732 9739 9747 9748 9752 9754 9755 9756 9757 9760 9763 9764 9765 9767 9770 9772 9774 9775 9777 9779 9782 9784 9785 9787 9788 9789 9793 9794 9795 9797 9799 9801 9802 9804 9805 9806 9808 9809 9810 9812 9813 9814 9815 9816 9817 9818 9819 9820 9821 9822 9823 9824 9825 9826 9827 9828 9829 9830 9831 9832 9833 9834 9836 9837 9838 9839 9840 9841 9860 9887 9891 9893 9894 9901 9902 9907 9908 9909 9916 9917 9922 9925 9934 9935 9937 9939 9941 9945 9946 9953 9954 9958 9959 9961 9963 9967 9991 10003 10004 10005 10006 10007 10008 10009 10010 10011 10012 10013 10018 10019 10020 10021 10022 10023 10024 10027 10029 10032 10060 10064 10070 10078 10079 10080 10082 10083 10084 10085 10086 10091 10092
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide distribution - USA nationwide, Austria, Australia, Belgium, Chile, Canada, Colombia, Ecuador, Egypt, Finland, France, Germany, Hungary, Iceland, India, Indonesia, Iraq, Italy, Japan, Libya, Netherlands, Norway, Panama, Peru, Portugal, Romania, Russia, Saudi Arabia, South Africa, Spain, Sweden, Thailand, Tunisia, Turkey, Ukraine, and United Kingdom.
  • Descripción del producto
    Servo-I ventilator system CO2 analyzer. Part number 65 23 588.
  • Manufacturer
  • Modelo / Serial
    0998-00-0800-31 0998-UC-0800-31 0998-00-0800-32 0998-UC-0800-33 0998-00-0800-33 0998-UC-0800-52 0998-00-0800-34 0998-UC-0800-53 0998-00-0800-35 0998-UC-0800-55 0998-00-0800-45 0998-00-0800-52 0998-00-0800-53 0998-00-0800-55.   CARDIOSAVE Hybrid IABPs serviced with a new/replacement power supply after August 19, 2014 are not affected.
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    US Nationwide distribution
  • Descripción del producto
    Maquet CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP)
  • Manufacturer
  • Modelo / Serial
    Part numbers BO-HMOD 70000, 70105.3815, BEQ-HMOD 70000, 70105,3824
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - US Nationwide and the countries of: Argentina, Australia, Austria, Belgium, Brazil, Bulgaria, Canada, China, Colombia, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Great Britain, Greece, Hungary, Iceland, Ireland, Israel, Italy, Japan, South Korea, Latvia, Lithuania, Luxembourg, Malta, Mexico, Netherlands, Norway, Poland, Portugal, Romania, Saudi Arabia, Serbia Montenegro, Singapore, Slovakia, Slovenia, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey and Uruguay
  • Descripción del producto
    Quadrox-iD Adult Diffusion Membrane Oxygenator || Product Usage: || The Quadrox-iD Adult Diffusion Membrane Oxygenator is intended for use in an extracorporeal circulation during cardiopulmonary bypass in cardiac surgery. Within the specified flow rate range, the device oxygenates the blood, removes carbon dioxide from the blood and regulates the blood temperature. The oxygenator with diffusion membrane cannot be used for the administration of volatile anesthetic gases because the gas molecules are unable to pass through the diffusion membrane. Responsibility for deciding whether to use an oxygenator rests solely with the attending physician.
  • Manufacturer
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