Radiometer immunoassay AQT90FLEX Analyser 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Radiometer Pacific 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-2015-RN-00273-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2015-03-27
  • 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
    Radiometer has recently become aware of a potential significant clinical issue where a measured parameter with a positive result may be reported as being negative.The problem may occur in rare situations where the analyser uses an incorrect hct value equal to 0% possibly due to:· incorrect needle calibration in wash block after change of hct cell. · needle not sufficiently tightened after replacement. insufficient cleaning causing disrupted flow in the fluid path between wash block and needle. · air bubbles in the sample due to use of a different sample tube than recommended.
  • 조치
    A Radiometer Pacific representative will perform a test to determine if the analyser is affected and perform a correction to eliminate the risk. A software update is under development that will include an analysis process check to eliminate the possibility of this error. End users are requested to ensure that the mandatory ‘System Clean’ is performed regularly as instructed in the AQT90FLEX Instructions For Use. This action has been closed-out on 26/08/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    Radiometer immunoassay AQT90FLEX AnalyserARTG Number: 224867An in vitro diagnostic medical device (IVD).
  • Manufacturer

Manufacturer