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) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 GE Healthcare IITS Australia Pty Ltd 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

의료기기에 문제가 생겼을 경우 제조사가 이를 바로잡거나 시장에서 회수하는 조치를 말한다. 회수(Recall)는 의료기기에 결함이 있거나, 건강에 위협이 되거나, 또는 결함도 있고 건강에도 위협이 될 경우에 발생한다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Recall
  • 사례 ID
    RC-2015-RN-01006-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2015-10-13
  • 사례 국가
  • 사례 출처
    DHTGA
  • 사례 출처 URL
  • 비고 / 경고
    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.
  • 데이터 추가 비고
  • 원인
    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.
  • 조치
    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

  • 모델명 / 제조번호(시리얼번호)
    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
  • 의료기기 분류등급
  • Manufacturer

Manufacturer