iPlan RT / iPlan RT Dose Radiation Treatment Planning Software used in combination with a localiser and one of the positioning solutions Target Positioner, ExacTrac v.4.5 or v.5.x, ExacTrac Vero (versions 2.1, 3.0, 3.1, 3.1.1, 3.2.0, 3.2.1) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Brainlab 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-2014-RN-01293-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2014-12-11
  • 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
    Incorrect patient positioning at the linac might occur, if all of the following conditions are met:1. at least two different ct datasets are being used and have been both localized and fused toeach other in the same treatment plan.2. the latest ct scan used with the localizer is not assigned as both reference set and alignmentset (for definitions, see the appendix).3. patients are positioned at the linac using one of the following positioning solutions:- target positioner- exactrac v.4.5 or v.5.X- exactrac vero (from v.2.1 up to v.3.2.1)the magnitude of potentially incorrect patient positioning is given by the difference in patient position inside the localizer during the two ct scans, one of which was assigned to the reference set and the other to the alignment set.
  • 조치
    1) Brainlab will provide existing potentially affected iPlan RT / iPlan RT Dose customers with this product notification information. 2) Brainlab will provide a software solution to prevent the described scenario from occurring. Brainlab will actively contact affected customers starting January 2016 to schedule the update. 3) Brainlab will refine the instructions for use of the iPlan RT treatment planning software in regard to implications of Alignment Set and Reference Set selections and will provide this user guide update to existing affected customers together with the software update. This action has been closed-out on 22/08/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    iPlan RT / iPlan RT Dose Radiation Treatment Planning Software used in combination with a localiser and one of the positioning solutions Target Positioner, ExacTrac v.4.5 or v.5.x, ExacTrac Vero (versions 2.1, 3.0, 3.1, 3.1.1, 3.2.0, 3.2.1)ARTG Number: 121114
  • 의료기기 분류등급
  • Manufacturer

Manufacturer