Events

Retiro De Equipo (Recall) de Device Recall da Vinci S / Si Surgical System IS2000 / IS3000, Camera Arm Drape

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 Intuitive Surgical, 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
    70777
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-1388-2015
  • Fecha de inicio del evento
    2015-03-16
  • Fecha de publicación del evento
    2015-04-06
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2015-12-03
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=134706
  • 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
    Drape, surgical - Product Code KKX
  • Causa
    Cloudy/waxy appearance with potential to transfer waxy substance to the patient, and potential for drape to tear.
  • Acción
    Firm issued field safety notice to all customers on March 16, 2015. Field safety notice includes acknowledgement form to be returned to recalling firm. A second letter was sent on May 12, 2015 to inform users that the date that the drape product unaffected by the issue will not be availalble untisl October/November 2015, not May 2015 as stated in the original communication.

Device

Device Recall da Vinci S / Si Surgical System IS2000 / IS3000, Camera Arm Drape
  • Modelo / Serial
    Product number 420022-02; da Vinci S Camera Arm Drape, 20 Pack.  Lot Numbers for Cloudy/Waxy issue: ALL lot numbers  Lot Numbers for Tear issue: D142205, D142205A, D142275, D142275A, D142315, D142325, D142335, D142345, D142345A, D142375, D142375A, D142385, D142485, D142625, D142625A, D142655, D142685, D142695, D142695A, D142765, D142765A, D142835, D142835A, D142905, D142905A, D142965, D142975, D143015, D143035, D143035A, D143105, D143115, D143175, D143175A, D143185, D143245, D143255, D143255A, D143315, D143315A, D143385, D143385A, D143445, D143445A, D143515, D143515A, D150085, D150085A, D150095, D150155, D150155A, D150215, D150215A, D150295, D150295A, D150355, D150365, D150365A, D150425, D150435, D150435A, D150515, D150515A, D150565, D150575, D150575A, D150645, D150655, D150655A, DA142625, DA142835, DA143315, DA143385, DA150295, DA150515
  • Clasificación del producto
    General Hospital and Personal Use Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution-Argentina, Australia, Austria, Belgium, Brazil, Bulgaria, Canada, Chile, China (including Hong Kong), Colombia, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, Finland, France, France, Germany, Greece, Iceland, India, Indonesia, Ireland, Israel, Italy, Japan, Kuwait, Lebanon, Luxembourg, Malaysia, Mauritius, Mexico, Monaco, Netherlands, New Zealand, Norway, Pakistan, Panama, Philippines, Poland, Portugal, Puerto Rico, Qatar, Romania, Russia, Saudi Arabia, Singapore, Slovakia, Slovenia, South Africa, South Korea, Spain, Sweden, Switzerland, Switzerland, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, United States, Uruguay, Venezuela, Vietnam.
  • Descripción del producto
    da Vinci S / Si Surgical System IS2000 / IS3000, Camera Arm Drape, 20 Pack. || Microtek Medical Equipment Drapes are to be used to cover a variety of surgical and non-surgical equipment in various settings throughout the clinical setting.
  • Manufacturer
    Intuitive Surgical, Inc.

Manufacturer

Intuitive Surgical, Inc.
  • Dirección del fabricante
    Intuitive Surgical, Inc., 1266 Kifer Rd Bldg 100, Sunnyvale CA 94086-5304
  • Empresa matriz del fabricante (2017)
    Intuitive Surgical Inc
  • Source
    USFDA