Retiro De Equipo (Recall) de Terumo CDI Blood Parameter Monitoring System 500(Heart lung bypass in line blood gas monitor module)

Según Department of Health, Therapeutic Goods Administration, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en Australia que fue producido por Terumo Australia 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-2016-RN-00487-1
  • Clase de Riesgo del Evento
    Class I
  • Fecha de inicio del evento
    2016-04-28
  • 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
    The bpm sensor head assembly’s thermistor, which provides the blood temperature value does not meet specification. this may cause inaccurate temperature measurement and inaccurate analyte display values. the thermistor measurement takes longer to reach actual temperature and temperature measurements at the extremes (18°c and 37°c) are the most inaccurate. lowest temperature displayed was about 19°c for the thermistor when a different thermistor measured the temperature near 15°c. highest temperature displayed was about 32°c when a different thermistor measured about 37°c. inaccurate temperature measurement could also cause inaccurate measurements of other bpm values including potassium (k+), po2, pco2, and ph. the algorithms for these parameters rely on temperature for the calculations. inaccurate measurement of these values could result in inappropriate patient management. there have been no reports of injury.
  • Acción
    Terumo is advising users they can either; - Stop using the affected devices and return them to Terumo for repair. A loan unit will be provided until the corrected devices can be returned, OR - Continue to use the affected devices only for HSTAT monitoring functions until the replacement parts are available. These functions are unaffected by the issue. Once the replacement sensor heads are available, the devices should be returned to Terumo for repair. This action has been closed-out on 10/05/2017.

Device

  • Modelo / Serial
    Terumo CDI Blood Parameter Monitoring System 500(Heart lung bypass in line blood gas monitor module)Catalogue numbers.: 500AHCT & 500AVHCTSerial numbers: 1899, 1948, 2473, 8001ARTG Number: 94012
  • Clasificación del producto
  • Manufacturer

Manufacturer