Artis Q and Artis Q zen systems (Fluoroscopic X-ray systems) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Siemens 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-00782-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2014-07-11
  • 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
    Siemens has i identified the following issues with the artis q and artis q zen systems:1. in certain circumstances the release of radiation is blocked in connection with an error with the large display, for example, where an image cannot be displayed on the large display. in rare cases the system misinterprets the status of the large display and blocks the release of radiation.2. in the case of installations configured with a hospital emergency power supply for the entire system, radiation release may be blocked due to a software error, because a non-existent emergency power situation is detected by mistake.3. the coupling of failures caused by an electronic control element might lead to a radiation abort.
  • 조치
    Siemens is providing a software patch to correct this issue. The software limits the blockage of radiation release to three seconds and the screen in the control room displays the message "No Xray, try again". After the next attempt, radiation can then be released without restriction. The software modification also prevents misinterpretation of the emergency power supply issue. An additional hardware signal supression component will be fitted to mitigate electronic control element failure. This action has been closed-out on 01/03/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    Artis Q and Artis Q zen systems (Fluoroscopic X-ray systems)Multiple material numbers with software VD10D and Large DisplayARTG Number: 102177
  • Manufacturer

Manufacturer