Retiro De Equipo (Recall) de Centricity PACS-IW with Universal Viewer Versions 5.0 SP2 and higher and Centricity Universal Viewer versions 6.0 and higher (used for storage and retrieval of images used in radiology)

Según Department of Health, Therapeutic Goods Administration, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en Australia que fue producido por GE Healthcare IITS 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-2015-RN-01006-1
  • Clase de Riesgo del Evento
    Class I
  • Fecha de inicio del evento
    2015-10-13
  • 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 products, when deployed with centricity pacs and centricity enterprise archive, or retrieving images from vendor neutral dicom archives, display inaccurate measurements on magnification views acquired from certain digital x-ray systems because certain scanner-originated magnification factors are not taken into account by universal viewer. specifically, distance measurements may not be calculated accurately when viewing projection radiography and fluoroscopy images that contain values in the imager pixel spacing (0018, 1164) and magnification factor (0018, 1114) dicom tags but does not contain a value in the pixel spacing (0028, 0030) tag. true size printing on film/paper for images produced by such modalities is also impacted. if known size fiducials are not present on the image and manual calibration is not possible, this can lead to an overestimation of distance measurements on the images. there have been no injuries reported as a result of this issue.
  • Acción
    For all projection X-rays, GE Healthcare recommends that the user perform the necessary measurements on the standard contact images, and not rely on measurements made on the magnified views unless the measurements have been independently verified for each X-Ray machine installed or manually calibrated using a radio-opaque fiducial of a known size. Attention should be given to prior cases acquired previously as they may be affected by the safety issue. GE Healthcare will correct all affected products.

Device

  • Modelo / Serial
    Centricity PACS-IW with Universal Viewer Versions 5.0 SP2 and higher and Centricity Universal Viewer versions 6.0 and higher (used for storage and retrieval of images used in radiology)ARTG Number: 161079
  • Clasificación del producto
  • Manufacturer

Manufacturer