XiO Software build versions 4.1 and higher (Radiation therapy treatment planning system) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Elekta 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-2014-RN-00275-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2014-03-03
  • 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
    Dose and monitor unit values are not computed correctly when elekta motorised wedges are used with dynamic conformal arcs. the problem occurs because only the start and stop angles of the dynamic conformal arcs are computed when all sub-beams of the arc should be computed. the planned dose distribution will not reflect the delivered dose. some anatomical structures will receive more dose than the plan reflects, some will receive less dose. it is possible that the target could likewise receive more or less dose than what is reflected in the plan. there is a remote probability of a mistreatment resulting in serious injury.
  • 조치
    Users are advised that the problem can be avoided by not using Elekta Motorised Wedges with Dynamic Conformal arcs. The problem was introduced in XiO Release 4.1 and will be resolved in Release 5.00.01 which will be released by March/April 2014.

Device

  • 모델명 / 제조번호(시리얼번호)
    XiO Software build versions 4.1 and higher (Radiation therapy treatment planning system)ARTG Number: 99769
  • 의료기기 분류등급
  • Manufacturer

Manufacturer