Dimension Vista 500 Intelligent Lab System and Dimension Vista 1500 Intelligent Lab System. An in vitro diagnostic medical device (IVD). 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Siemens Healthcare Pty 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-2017-RN-00347-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2017-03-14
  • 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
    There has been confirmation that in isolated cases when enzymatic creatinine (ecrea) is processed immediately after the weekly automated acid clean routine during probe test, there is the remote potential for an elevation of greater than 15 percent in the ecrea result. whilst it is understood that users routinely run quality control (qc) after system maintenance, it is particularly important to run ecrea qc after the probe test to identify a potentially elevated ecrea result. (please note that this information applies only to laboratories processing enzymatic creatinine (ecrea: enzymatic creatinine cat no. k1270a, smn 10700444) after the implementation of the automated acid clean (acln) maintenance routine).
  • 조치
    Siemens is recommending affected users to adhere to the following steps: 1) replace the appropriate reagent probe (only if the ECREA reagent probe has not been replaced since the activation of ACLN) 2) process QC which includes ECREA immediately after routinely scheduled Off Peak Activities including Probe Test; and 3) contact Siemens Customer Care Centre IF, after replacement of reagent probe, users experience elevated ECREA QC results directly after Off Peak Activities which includes the Probe Test or after manually processing the Probe Test.

Device

  • 모델명 / 제조번호(시리얼번호)
    Dimension Vista 500 Intelligent Lab System and Dimension Vista 1500 Intelligent Lab System. An in vitro diagnostic medical device (IVD).Dimension Vista 500 Intelligent Lab System Siemens Material Number (SMN) 10488224Dimension Vista 1500 Intelligent Lab SystemSiemens Material Number (SMN) 10444802ARTG number: 174699
  • Manufacturer

Manufacturer