Events

Retiro De Equipo (Recall) de Device Recall Alaris PC unit, model 8015

Según U.S. Food and Drug Administration, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en United States que fue producido por CareFusion 303, Inc..

¿Qué es esto?

Una corrección al equipo o acción de retiro tomada por el fabricante para abordar un problema con un dispositivo médico. Los retiros (recalls) ocurren cuando un dispositivo médico está defectuoso, cuando puede poner en riesgo la salud, o cuando simultáneamente está defectuoso y puede poner en riesgo la salud.

Más información acerca de la data acá
  • Tipo de evento
    Recall
  • ID del evento
    65564
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1835-2013
  • Fecha de inicio del evento
    2013-06-17
  • Fecha de publicación del evento
    2013-08-02
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2014-05-20
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=119581
  • Notas / Alertas
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Notas adicionales en la data
    Pump, infusion - Product Code FRN
  • Causa
    Carefusion is recalling the alaris pc units model 8015 (pc unit), version 9.12, because it is operating at an incorrect voltage and it could potentially experience a loss of communication between the pc unit main processor and keyboard processor.
  • Acción
    The firm, Carefusion, sent an "URGENT MEDICAL DEVICE RECALL NOTIFICATION" letter dated June 17, 2013 to all customers who purchased the Alaris PC unit (model 8015) with version 9.12-Keyboard Processor. The recall letter informs the customers of the problems identified and the actions to be taken. The customers were instructed to either discontinue use of affect PC units until remediated or continue use on patients and follow the steps provided in the letter; fully charge Alaris PC units prior to use; during operation and when not in transport, keep Alaris PC units plugged in at all times; consider having additional back up Alaris PC units available and if you experience the described error code messages on the Alaris PC unit during infusion, you may continue the infusion(s) as programmed unless a programming change is required. Obtain a back-up Alaris PC unit to replace the device. In addition, if the customer experiences a SYSTEM ERROR (111.2000 or 111.2002), or a CHANNEL DISCONNECTED error on the Alaris PC unit contact CareFusion Customer Advocacy at 888-812-3266; 24 hours a day, 7 days a week; email: customerfeedback@carefusion.com. The customers were also instructed to promptly complete and return the enclosed Customer Response Card. CareFusion will provide an update to correct the voltage on the keyboard processor for those affected Alaris PC units. Carefusion will contact all affected customers within 60 days to initiate the scheduling process for the remediation. Customers are instructed to contact CareFusion Support Center at (888) 562-6018 or at supportcenter@carefusion.com for recall related questions; hours 7:00am to 4:00pm PT, Monday-Friday. For adverse reports, customers are instructed to contact Customer Advocacy at (888) 812-3266; 24 hours a day, 7 days a week or at customerfeedback@carefusion.com. For Technical questions, customers are instructed to call (888) 812-3229; hours 6:00pm to 5:00pm PT, Monday-Friday or at dl-us-inf-techsupport@ca

Device

Device Recall Alaris PC unit, model 8015
  • Modelo / Serial
    1005435 10038007 1300550 3894703 1003149 19995706 3895887 19995118 1022500 1257000 1010235 3894799 1264612 1029800 10032389 3894714 3894796 1039450 19995610 3894886 1058150 1129100 1003197 1065900 3894701 10063252 1610200 1074200 3894708 10142044 1296030 1020387 3894811 1083900 10115320 1101500 1102400 1101601 10038966 19995620 3894841 1123000 1135600 1137240 1353400 3894860 1547000 1008565 1186900 6169100 10008460 3894844 1155500 3894711 10032361 10166465 3894702 10046069 10037661 10037647 3894834 3894836 10034261 1297400 1302600 1053000 1317801 3894817 3894797 10163092 10053161 1012161 3895854 10046578 1369040 1005333 1375900 10001956 3894734 3894789 3894833 10047157 1403100 1408700 10010196 3894892 3894765 1433251 1009496 1446000 1438800 1865900 1911872 10010570 19996156 10033408 1589480 1453703 1466600 1453702 6273300 10011620 1470203 1477201 1765300 1025650 10037131 19995384 1915200 1470204 1315403 10044246 1470001 1470202 19995746 6129700 1726300 1505700 10063253 10037742 1131700 10037723 4513601 1520101 1001799 10010451 4538200 10122836 1001783 1553400 1220200 3894705 1907800 1000456 6572500 19996529 10038213 3894830 1843701 10165568 1579040 10035744 10060127 3894819 3895895 1027700 1623400 1012793 10149088 3894849 1492500 1719500 10033426 1677100 1697501 1703300 6237701 1716400 1018653 10011474 1725100 1724300 1252400 6598300 1738700 6606300 10002540 19995700 10047163 1793108 3894718 1797801 10038591 1016746 1079000 1442503 19995670 10032641 1043750 1015768 1812600 1813200 1833900 1842600 1846801 1838401 1027503 1846000 10046982 10049664 10049674 10042072 10158492 10040131 1845700 3872400 3894825 3895883 3894801 3880600 3894722 3894716 3894723 3895875 3888400 6840950 10036536 3894870 1908600 1037000 1012361 19995045 10165422 10165005 10005354 10011455 1933600 3894735 1944700 980 500 10167738 111 10161003 10001154
  • Clasificación del producto
    General Hospital and Personal Use Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide distribution: US (nationwide) and countries of: Australia, Canada and Europe.
  • Descripción del producto
    Alaris PC unit, model 8015, with version 9.12-Keyboard Processor and logic board assembly part number TC10006584. || The Alaris PC Unit is the main user interface unit and power supply of the Alaris System, a modular system to be used with Alaris System modules intended for use in todays growing professional healthcare environment for facilities that utilize infusion and/or monitoring devices.
  • Manufacturer
    CareFusion 303, Inc.

Manufacturer

CareFusion 303, Inc.
  • Dirección del fabricante
    CareFusion 303, Inc., 10020 Pacific Mesa Blvd, San Diego CA 92121-4386
  • Empresa matriz del fabricante (2017)
    Becton, Dickinson and Company
  • Source
    USFDA