Events

Artis one 의 리콜

New Zealand Medicines and Medical Devices Safety Authority에 따르면, 해당 리콜 는 New Zealand 에서 Siemens Shenzhen Magnetic Resonance 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
    21595
  • 사례 시작날짜
    2017-06-28
  • 사례 국가
    New Zealand
  • 사례 출처
    NZMMDSA
  • 사례 출처 URL
    https://medsafe.govt.nz/hot/Recalls/RecallSearch.asp
  • 비고 / 경고
    Data from New Zealand is current through July 2018. All of the data comes from the New Zealand Medicines and Medical Devices Safety Authority, 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 New Zealand.
  • 데이터 추가 비고
    Recalling Organisation: Siemens Healthcare (NZ) Ltd, Millennium Centre, Part Level 2, Building A, 600 Great South Road, Ellerslie, AUCKLAND 1051
  • 원인
    The wannacry ransomware attack was a worldwide cyberattack by the wannacry ransomware cryptoworm, which targeted computers running the microsoft windows operating system by encrypting data and demanding ransom payments in the bitcoin cryptocurrency. many of the systems are utilizing windows xp and windows 7 operating systems and therefore are at risk from wannacry virus. the manufacturer has released security patches as correction to address this issue, however the medical device is still performing according to its specifications and security patches are only cybersecurity enhancements.
  • 조치
    Software to be upgraded

Device

Artis one

Manufacturer

Siemens Shenzhen Magnetic Resonance Ltd