UniCel DxC ISE Reference reagent tubingUniCel DxC 600/800 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-2015-RN-00697-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2015-08-03
  • 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
    Beckman coulter has identified a failure of the unicel dxc ise tubing (lines 11, 25 and 26) for ise reference reagent. the failure occurs due to the interaction between a new tubing plasticiser and the ise reference reagent. the supplier's change in plasticiser was due to a move to a phthalate-free tubing material based on new environmental regulations. as a result, a visible slow-forming non-microbial white material may appear inside the tubing. this may result in suppressed ise quality control and patient results due to reference drift errors and/or ise calibration failures and/or tubing lines 25 or 26 detaching due to obstruction of flow.
  • 조치
    Users are requested to immediately perform a visual inspection of ISE Reference reagent tubing 11, 25, and 26 for the white material and in cases where material is identified a workaround is provided. In the longer term, Beckman Coulter is qualifying new ISE tubing and laboratories will be notified when new tubing is available to be installed on instruments subject to this Recall. This action has been closed-out on 02/05/2017.

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