Retiro De Equipo (Recall) de AQURE Data Management System Software prior to version 1.8.2 may be affected.

Según Department of Health, Therapeutic Goods Administration, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en Australia que fue producido por Radiometer Pacific 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-2014-RN-00453-1
  • Clase de Riesgo del Evento
    Class II
  • Fecha de inicio del evento
    2014-04-17
  • País del evento
  • Fuente del evento
    DHTGA
  • URL de la fuente del evento
  • 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
    Radiometer has recently become aware of three potential issues with unit conversion in aqure that may occur if the device is transmitting in a different unit than aqure is displaying and/or transmitting to the his/lis. - conversion of ketone from mmol/l to mg/dl or vice versa: the parameter ketone is measured on either the siemens clinitek or the docureader. this is not applicable in australia as none of these devices are connected to aqure. - conversion of glucose and lactate from g/l to mmol/l or vice versa: in both cases a potential wrong conversion factor may be used, which may cause the reported result to be incorrect by a factor 10,000. this problem may be present in all versions of aqure.- converting from mg/dl to mg/l and g/dl to g/l or vice versa: a potential wrong conversion factor may be used of 1/10. the correct factor is 10. reported results may be incorrect by a factor 100. this problem is not parameter specific and may be present in all versions of aqure.
  • Acción
    End users are requested to not change the units on AQURE or iSTAT without consulting Radiometer Pacific. Radiometer will be carrying out testing to identify affected software and a software update will be installed to correct the issue. This action has been closed-out on 29/01/2016.

Device

  • Modelo / Serial
    AQURE Data Management SystemSoftware prior to version 1.8.2 may be affected.
  • Manufacturer

Manufacturer