Siemens Advia Centaur XPT 의 리콜

New Zealand Medicines and Medical Devices Safety Authority에 따르면, 해당 리콜 는 New Zealand 에서 Siemens Healthcare Diagnostics Inc 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
    18951
  • 사례 시작날짜
    2015-08-03
  • 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, 55 Hugo Johnston Drive, Penrose, Auckland
  • 원인
    Siemens healthcare diagnostics has identified multiple issues with the advia centaur® xpt system software v1.0.1 (bundle 1.0.912 smn 10819704) and v1.0.2 (bundle 1.0.1086 smn 11219806)., when running thcg samples with an initial dilution of 1 to 200, without processing neat specimens, it is potentially possible to miss a positive thcg value where the neat value is less than 1000. a lookback of 48 hours is recommended for negative thcg samples if neat values were not initially run for thcg and large dilutions were employed., there is the extremely unlikely potenial to transpose patient results when running in rack order mode without positive sample identificiation., similarly a lookback of 48 hours for any instruments running in this mode is recommended.
  • 조치
    Software to be upgraded

Device

Manufacturer