Access Free T3 Reagent Kit (used in the diagnosis and monitoring of patients with thyroid disorders). An in vitro diagnostic medical device (IVD) 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-2016-RN-00818-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2016-06-17
  • 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
    Beckman coulter has determined through customer feedback and internal testing that the access free t3 reagent lots demonstrate an upward shift in patient results. the preliminary results indicate this upward shift may be related to a june 2015 formulation design change that was introduced to improve the access free t3 open reagent pack stability. the upward shift in patient test results, therefore, is expected to be maintained for all future lots. patient sample results will shift upward by approximately 10-14% across the reference interval when compared to the results generated with reagent lots manufactured prior to the june 2015 design change. due to matrix differences, qc values may not demonstrate a shift.
  • 조치
    Beckman Coulter is advising users to discontinue use of the affected product and either verify the current Free T3 references interval(s) are appropriate or adjust or establish new reference intervals(s). Use of the affected lots can be resumed once the reference intervals have been evaluated. A review of previously generated results and clinical notification is at the discretion of the Laboratory Director. This acrtion has been closed out on 16 June 2017.

Device

  • 모델명 / 제조번호(시리얼번호)
    Access Free T3 Reagent Kit (used in the diagnosis and monitoring of patients with thyroid disorders). An in vitro diagnostic medical device (IVD)Reference Number: A132422Multiple lot numbers affectedARTG Number: 213976
  • Manufacturer

Manufacturer