Events

Retiro De Equipo (Recall) de qube Compact Monitor & XPREZZON Bedside Monitorqube Compact Monitor shipped between 16 December 2013 and 15 December 2014

Según Department of Health, Therapeutic Goods Administration, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en Australia que fue producido por Medtel Pty Ltd.

¿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
    RC-2015-RN-00104-1
  • Clase de Riesgo del Evento
    Class II
  • Fecha de inicio del evento
    2015-02-06
  • País del evento
    Australia
  • Fuente del evento
    DHTGA
  • URL de la fuente del evento
    https://apps.tga.gov.au/Prod/sara/arn-detail.aspx?k=RC-2015-RN-00104-1
  • Notas / Alertas
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, 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 Australia.
  • Notas adicionales en la data
  • Causa
    Spacelabs healthcare has received multiple reports regarding the following: - a failure to boot following power on or reset, resulting in monitor operation.- loss of network connectivity, which may result in;- an inability to display alarms and data from the affected monitor on central stations and other bedside monitors, or- a failure to transmit parameter and alarms from the affected monitor to system printers and sapcelabs’ intesys clinical suite retrospective database (including the clinical events interface remote notification feature).- display of english language when previously configured for another language (the alarm messages displayed in the parameter waveform zone are not affected as these are stored on a command module and not on the monitor.- touchscreen failure where touching the screen does not produce the expected response.This issue is caused by inadequate electrical contact on one of the printed circuit board assemblies.
  • Acción
    A small number of printed circuit boards with the affected socket were also distributed to customers to facilitate repair of customer monitors. Medtel Pty Ltd will contact affected customers to schedule a convenient time to replace the PCBAs in in their facility. Meanwhile customers are advised the following: - The reported issues occur mostly at initial power on of a monitor. Always check for proper operation (such as functionality of touchscreen, proper language, and network connectivity) when the monitor is first turned on. - If the product is monitored via a central station, ensure the notification feature for monitoring communication loss is on. The capability is on by default. - If a bedside monitor is not monitored via central station, check the bedside monitor frequently to ensure the display is functional. - Do not rely solely on the monitor for critically ill patients. This action has been closed-out on 05/08/2016.

Device

qube Compact Monitor & XPREZZON Bedside Monitorqube Compact Monitor shipped between 16 December 2...
  • Modelo / Serial
    qube Compact Monitor & XPREZZON Bedside Monitorqube Compact Monitor shipped between 16 December 2013 and 15 December 2014Catalogue number: 91390ARTG number: 108755XPREZZON Bedside Monitor shipped between 18 June 2014 and 13 January 2015Catalogue number: 91393ARTG number: 181195
  • Manufacturer
    Medtel Pty Ltd

Manufacturer

Medtel Pty Ltd
  • Source
    DHTGA