MIA FORA NGS HLA Server and Software versions 3.0 and 3.1. An in vitro diagnostic medical device (IVD) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Abacus dx 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-2018-RN-00403-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2018-05-16
  • 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
    The following issues have been identified with mia fora ngs hla server and software versions 3.0 and 3.1:1. an anomaly in the mia fora ngs software involving the mismatch in exon (mme) column of the allele candidate table for drb1,3,4,5 and dqb1;2. class i hla-a primers do not cover the complete 5' and 3' untranslated regions (utr) as described in the imgt database;3. for class ii, the reverse primers for dpb1 overlap a few bases on exon 4; the reverse primer for dpa1 overlaps the last few bases of the 3' end of exon 4; exon 6 of dqb1 is not included in the amplified product; and4. the lack of polymorphisms in a region of certain allele combinations of hla class i genes may make it challenging to determine the correct phasing for heterozygous samples.
  • 조치
    Abacus is advising customers that the issues will be corrected in the next revision of the MIA FORA NGS FLEX Software which will include a revised Package Insert to clarify existing or add additional assay limitations. It expected that this software will be released in August 2018. Until the next revision is available, users should refer to the Appendix provided with the Customer Letter to manually review results.

Device

  • 모델명 / 제조번호(시리얼번호)
    MIA FORA NGS HLA Server and Software versions 3.0 and 3.1. An in vitro diagnostic medical device (IVD)MIA FORA NGS HLA Server, Linux SR-790-00017 or Windows SR-790-00020MIA FORA NGS Software, Linux SR-850-00043, Windows SR-850-00062 or Registry SR-790-00068ARTG Number: 288607(Abacus dx Pty Ltd - Interpretive software IVDs)
  • Manufacturer

Manufacturer