IH-1000 (immuno-haematology instrument). An in vitro diagnostic medical device (IVD) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Bio-Rad Laboratories 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-2014-RN-01195-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2014-11-10
  • 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
    Further to a customer complaint, bio-rad have confirmed that in the specific conditions detailed below, the ih-1000 software may lose the link sample/”test in progress”. this loss might lead to a mismatch between the test result and the patient sample.This issue is linked to the sample management when using the “emergency* button” and might occur only in the following conditions:- a not urgent rack (green label) is inserted with more than one sample and;- all the samples on this rack are manually selected as “emergency” by clicking on the “emergency* button”;then once the first emergency sample is processed, the instrument ejects the rack before all processing is completed.- if a rack is then reloaded with new samples in the exact same positions and reinserted in the same slot, the link sample/”test in progress” is lost.
  • 조치
    This issue will be permanently corrected in the next IH-1000 software version. This version will be released by the end of Q1 2015. In the meantime, customers should immediately discontinue using the “emergency button” and should process all emergency samples exclusively on the urgent rack.

Device

  • 모델명 / 제조번호(시리얼번호)
    IH-1000 (immuno-haematology instrument). An in vitro diagnostic medical device (IVD)Catalogue Number: 001000VAffected Version - All SoftwareARTG number: 184446
  • Manufacturer

Manufacturer