Retiro De Equipo (Recall) de Siemens AXIOM Artis, Artis zee and Artis Q/Q

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 Siemens AG.

¿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
  • ID del evento
  • Fecha de inicio del evento
  • País del evento
  • Fuente del evento
  • 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: Siemens Healthcare (NZ) Ltd, Millennium Centre, Part Level 2, Building A, 600 Great South Road, Ellerslie, AUCKLAND 1051
  • Causa
    Due to a leak in the cooling system, fluids could seep into the equipment cabinet. this leak can occur sporadically in the affected systems., manufacturer initiated two field safety corrective actions (ax004/15/s und ax060/15/s) to address the issues with two different vendors for detector cooling devices. as the issues are identical, locally manufacturer sending both letters with one cover letter to all affected customers (this will prevent confusion among customers that have multiple systems and were required to receive both letters). each affected system will receive only one correction depending on the system type.
  • Acción
    Product to be modified


  • Modelo / Serial
    Model: 7555365,10094141,10094139,10094137,10094135,10280959,10848281,10848280,10848282,7413078,7412807,7008605,10848355,7728392,7555357,7727717, Affected:
  • Manufacturer


  • Empresa matriz del fabricante (2017)
  • Source