NucliSENS easyMAG Magnetic Silica MagSIL (used with the NucliSENS easyMag nucleic acid extraction system for the automated extraction of total nucleic acids (RNA/DNA) from biological samples). An in vitro diagnostic medical device (IVD) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Biomerieux 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-00949-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2016-07-20
  • 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
    Following customer complaints about amplification performance issues with home brew pcr and rt- pcr assays, biomérieux investigation has confirmed an issue with specific batches of magnetic silica (ref: 280133). the investigation concluded that downstream applications were impacted when the extraction volume was higher than 400µl and for double stranded nucleic acids target. double stranded nucleic acid applications with small (< 40kbp) and medium genome sizes (< to 1200 kbp) i.E., dna viruses are more impacted than higher human genomic dna and bacterial applications (> to 1200kbp).This may result in false negative, invalid or under-quantification of results. if invalid results are obtained, it could lead to a delayed result until a new run or a new extraction is performed.
  • 조치
    bioMérieux is advising users to ensure controls with the same nature/structure as the target and/or external controls are used to detect the issue. Users are advised to reduce the sample input volume to 200µL, until the silica problems is resolved. Downstream ARGENE and NucliSENS easyQ HIV 1 V2.0 applications performed according to the IFU are not affected. It is recommended that the continued use with blood transfusion testing with confirmed by the Laboratory Director, and to discuss any concerns regarding previously reported results with the Laboratory Director.

Device

  • 모델명 / 제조번호(시리얼번호)
    NucliSENS easyMAG Magnetic Silica MagSIL (used with the NucliSENS easyMag nucleic acid extraction system for the automated extraction of total nucleic acids (RNA/DNA) from biological samples). An in vitro diagnostic medical device (IVD)Catalogue Number: 280133Lot Numbers:Z017BB1MS, Z017BF1MS, Z017BA1MS Expiry Date: 28/02/2017Z017CC1MS, Z017CG1MS Expiry Date: 28/03/2017Z017DC1MS, Z017DD1MSExpiry Date: 28/04/2017ARTG Number: 240760
  • Manufacturer

Manufacturer