RayStation software versions 2.5, 3.0, 3.5, and 4.0 (radiation therapy treatment planning system) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Emergo Asia Pacific Pty Ltd T/a Emergo Australia 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-2014-RN-00144-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2014-02-12
  • 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
    This notice concerns an issue found with the hybrid deformable registration in raystation 2.5, 3.0, 3.5, and 4.0. rigid registration is a standard first step prior to running a hybrid deformation. the rotation component of the rigid registration computed prior to the deformable registration is not accounted for in fusion views when mapping structures (regions or points of interest) or when deforming dose.
  • 조치
    Emergo is advising their customers to ensure that the "discard rotation" option is selected in the Image Registration Module before creating a rigid registration intended to be used for hybrid deformable registration. End users can also use the ROI based deformable registration when applicable as this functionality is not affected by the error. A software patch will be release to correct this problem.

Device

Manufacturer