4D Integrated Treatment Console (4DITC) Version: 10 and 11 (Used for accurate treatment delivery by monitoring linear accelerator parameters) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Varian Medical Systems Australasia 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-00947-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2014-08-29
  • 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
    Varian received two reports from customers with c-series linear accelerators (linac) used with varian’s barcode conical collimator verification system (bccv) and brainlab’s exactrac patient positioning system where the user was able to clear the interlock for bccv, imposed by the 4ditc, from the exactrac console. in both reported cases, the user was employing a c-series he linac with 4ditc and both exactrac and bccv. the user was authorising the exactrac to the linac 4ditc. successive signals were sent from the exactrac to the 4ditc. the first signal cleared the exactrac interlock as intended. the exactrac console requested user confirmation of the second command to authorise. the user responded affirmatively. the signal was sent to the 4ditc, and the linac interlock associated with bccv was released. in such a situation, it may be possible to irradiate the patient using a cone other than what is specified by the treatment plan because the bccv verification was not completed.
  • 조치
    Varian is reminding users of the correct procedures using auxiliary devices requiring the ADI interface and is providing recommended verification steps when carrying out treatment i.e., stereotactic radiosurgery (SRS) or stereotactic body radiation therapy (SBRT). A permanent fix has been developed and a Varian representative will schedule the installation. This action has been closed-out on 12/08/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    4D Integrated Treatment Console (4DITC) Version: 10 and 11 (Used for accurate treatment delivery by monitoring linear accelerator parameters)Product code: H51Serial Numbers: H514278, H514544, H515102, H51B568, H513894, H515619 & H51B100ARTG Number: 116839
  • 의료기기 분류등급
  • Manufacturer

Manufacturer