Siemens syngo.Plaza Imaging System 의 리콜

New Zealand Medicines and Medical Devices Safety Authority에 따르면, 해당 리콜 는 New Zealand 에서 Siemens AG 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
    17987
  • 사례 시작날짜
    2016-01-14
  • 사례 국가
  • 사례 출처
    NZMMDSA
  • 사례 출처 URL
  • 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
    In case of a system crash images may not be written to the hard disk and there may be inconsistencies in the database. when a system crash occurs (e.G. blue screen, power outage), images may not be written from cache to the hard disk and are lost. in such a case an existing file name identifier might be re-used after restart of the system. now two references to the same image file on sts exist in the database of syngo.Plaza., manufacturer has now released another version of the software as a final correction to this this action (sy099/14/s) . this software update will fix any inconsistencies in the archived data that may have occurred before software update vb10a_hf06 was installed.
  • 조치
    Software to be upgraded

Device

  • 모델명 / 제조번호(시리얼번호)
    Model: Catalogue Number: 10863171 & 10592457, Affected: , Software version: All versions
  • Manufacturer

Manufacturer