Siemens Advia Centaur XPT System 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
    18832
  • 사례 시작날짜
    2015-07-09
  • 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
    Siemens healthcare diagnostics has identified the following issue on the advia centaur® xpt system :, · the time of initiation for onboard stability (obs) on the advia centaur® xpt system is calculated when probe wash reagent packs are pierced (used by the system), not when loaded onto the instrument, for probe wash reagents pw2, pw3 and pw4., · because onboard stability (obs) is calculated when the probe wash reagent pack is pierced, not when loaded onto the instrument, the probe wash reagent pack may be on the instrument longer than described in the instructions for use (ifu).
  • 조치
    Instructions for use to be updated

Device

  • 모델명 / 제조번호(시리얼번호)
    Model: 10711433, Affected: All serial numbers manufactured from Oct-2014 to Feb-2015
  • Manufacturer

Manufacturer