Retiro De Equipo (Recall) de GE DashPort 2 Patient Monitor

Según New Zealand Medicines and Medical Devices Safety Authority, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en New Zealand que fue producido por GE Medical Systems Information Technologies.

¿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
    13319
  • Fecha de inicio del evento
    2012-08-14
  • País del evento
  • Fuente del evento
    NZMMDSA
  • URL de la fuente del evento
  • Notas / Alertas
    Data from New Zealand is current through July 2018. All of the data comes from the New Zealand Medicines and Medical Devices Safety Authority, 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 New Zealand.
  • Notas adicionales en la data
    Recalling Organisation: GE Healthcare Limited, 8 Tangihua Street, Auckland 1010
  • Causa
    The manufacturer had advised that there are several potential issues with the dash 3000/4000/5000 patient monitors;, 1/ dash stops communication on the unity network resulting in loss of monitoring at the centra station, 2/ dash displays distorted ecg waveform in combination monitoring mode, 3/ dash incorrectly becomes time master on the unity network, 4/ dash date reverts to 1993, 5/ dashport 2 stops communicating on the unity network resulting in loss of monitoring at the central station.
  • Acción
    Software to be upgraded

Device

Manufacturer