Retiro De Equipo (Recall) de GAS/WATER FEEDING VALVE- OF-B194

Según Health Canada (via FOI), este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en Canada que fue producido por PENTAX CANADA 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
    15660
  • Clase de Riesgo del Evento
    I
  • Fecha de inicio del evento
    2013-09-05
  • País del evento
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Notas adicionales en la data
  • Causa
    Pentax upper/lower g.I. endoscopes are provided with an air/water valve. as an alternative the optionally available of-b194 gas/water feeding valve may be used in place of the standard air/water valve to deliver a non-explosive gas (c02) for insufflation. we have been informed about a product issue involving the of-b194 gas/water feeding valve. the reported defect may cause improper stoppage of the supply of co2 gas during an endoscopic procedure with the potential for serious hazard to the patient (i.E. increased risk of perforation due to continuing flow of co2 gas). pentax medical has discovered a manufacturing assembly failure which cannot be corrected at the user facility and therefore the of-b194 gas/water feeding valve must be removed from use immediately.

Device

Manufacturer

  • Dirección del fabricante
    MISSISSAUGA
  • Empresa matriz del fabricante (2017)
  • Source
    HC