Access 2 Family of Immunoassay Systems. An in vitro diagnostic medical device (IVD) Access 2, Access 2, Re-manufactured and the UniCel DxC 600i SYNCHRON Access Clinical Systems 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Beckman Coulter Australia 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-00369-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2017-03-17
  • 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
    It has been determined that a circuit board that controls motor functions in specific instrument systems can affect device positioning on the pipettor and incubator belt while the instrument is running. users may experience the following errors that may cause a delay in the reporting of patient results: - an incubator belt motion error which can result in the instrument going into the not ready mode and cancellation of all in-process tests; and/or - z pipettor motion errors which can result in cancelled tests.In the worst case scenario, the potential harm would be a delay in patient diagnosis and/or treatment, with a potential worst case severity of permanent injury. the probability of harm for this event is unlikely.
  • 조치
    Beckman Coulter (BC) is advising users to adhere to the following interim instructions. If you experience: - z pipettor motion errors, to re-run any cancelled tests; and/or - incubator belt motion errors. please review the associated event on the ‘Event Log’ screen and follow the troubleshooting instructions provided. Users are further advised that they will be contacted by their BC service representative to schedule a visit to replace the circuit board on their instruments as a permanent fix.

Device

  • 모델명 / 제조번호(시리얼번호)
    Access 2 Family of Immunoassay Systems. An in vitro diagnostic medical device (IVD)Access 2, Access 2, Re-manufactured and the UniCel DxC 600i SYNCHRON Access Clinical SystemsReference Numbers: 81600N, 386220, A25637, A25638 Multiple Instrument Serial NumbersARTG Number: 177999
  • Manufacturer

Manufacturer