Events

Retiro De Equipo (Recall) de ADVIA Centaur and ADVIA Centaur XP HBsAg II Assay. An in vitro diagnostic medical device (IVD)

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

¿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-2012-RN-01292-1
  • Clase de Riesgo del Evento
    Class II
  • Fecha de inicio del evento
    2012-12-24
  • 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-2012-RN-01292-1
  • 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
    There is an increased number of falsely elevated patient samples for hbsagii resulting in the number of initial positives reactive rates exceeding the initial reactive specificity as listed in the instructions for use (ifu). the increased false reactive rate may cause a delay in reporting results because additional testing is required.
  • Acción
    Siemens is providing work around instructions for users to implement.

Device

ADVIA Centaur and ADVIA Centaur XP HBsAg II Assay. An in vitro diagnostic medical device (IVD)
  • Modelo / Serial
    ADVIA Centaur and ADVIA Centaur XP HBsAg II Assay. An in vitro diagnostic medical device (IVD)ADVIA Centaur and ADVIA Centaur XP HBsAg II (HBsII) AssayReference Number: 10492138Kit Lot numbers: 93076013, 94615013, 95344013, 95801013, 96628013, 98117014, 98508014, 12536014An in vitro diagnostic medical device (IVD)
  • Manufacturer
    Siemens Ltd Diagnostics Division

Manufacturer

Siemens Ltd Diagnostics Division
  • Empresa matriz del fabricante (2017)
    Siemens AG
  • Source
    DHTGA