Elekta Integrity R3.0 Digital Linear Accelerator 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-2013-RN-00375-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2013-04-30
  • 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
    The problem is that the "static tolerances" from the calibration files (loaded database) are used for beam delivery instead of the machine calculated values. a fault will occur is the loaded database is incorrect, and could cause clinical mistreatment.
  • 조치
    Elekta is advising that the solution to this problem is to upgrade to IntegrityR3.1 as soon as it is available. An updater tool will be available within the next few months and will be Field Safety Modification number 200 02 502 030. This tool is a CD disk that Elekta Service will use on each product to check tolerances and it will adjust if necessary. This is a one-time check unless there is a change to the configuration, such as a new license for the LINAC and then a new check will be needed.

Device

  • 모델명 / 제조번호(시리얼번호)
    Elekta Integrity R3.0 Digital Linear AcceleratorARTG Number: 191025
  • Manufacturer

Manufacturer