ECLIPSE TPS V8.8 의 리콜

Health Canada (via FOI)에 따르면, 해당 리콜 는 Canada 에서 VARIAN MEDICAL SYSTEMS INC. 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
    79362
  • 사례 위험등급
    II
  • 사례 시작날짜
    2012-04-30
  • 사례 국가
  • 사례 출처
    HC
  • 비고 / 경고
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • 데이터 추가 비고
  • 원인
    The energy shown or selected by the treatment planner in the 'fields' tab of the external beam planning (ebp) and in the 'general' tab of field properties may differ from the value actually used for dose calculation. caused by incorrect handling of the energy mode object within the memory cache system used by eclipse external beam planning version 10. when the user changes field energy the memory cache anomaly may result in use of previously selected field energy instead of intended field energy. this cache memory issue may arise when switching between software applications (such as between external beam planning and rt chart) when using multiple sessions or when switching between patients in a single session of ebp in eclipse.

Device

  • 모델명 / 제조번호(시리얼번호)
    Model Catalog: 100042024 (Lot serial: >10 SERIAL NUMBERS.); Model Catalog: 100042024 (Lot serial: CONTACT MANUFACTURER.)
  • 제품 설명
    Eclipse Treatment Planning System V8.8
  • Manufacturer

Manufacturer