AFB III Staining Kit (An in vitro diagnostic medical device (IVD)) (Qualitative histologic stain to selectively indicate Mycobacterium and other acid fast organisms) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Roche Diagnostics Australia Pty Limited 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-01161-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2014-10-29
  • 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
    Roche diagnostics has observed a staining artefact on slides stained with the afb iii staining kit. this artefact consists of a circular and a non-specific purple- to pink-coloured slide background staining, which in some cases is present within tissue elements and in other cases takes the form of circular deposits that appear to be above the tissue plane. the latter can occur both within the tissue-containing and blank portions of the slide. this artefact may interfere with the interpretation and identification of acid-fast bacteria, which is the indication for this assay. also, the artefact could be mistaken for acid-fast bacteria and lead to a false positive interpretation. a trained pathologist would recognise the artefacts and reject the slide without attempting to interpret it.
  • 조치
    Roche Diagnostic Australia Pty Ltd is requesting the customers to identify and discard the affected lots and is providing credit for the affected lots that are discarded. Roche Diagnostic is also requesting the customers to consider the need to review patient results using the affected lots. This action has been closed-out on 12/08/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    AFB III Staining Kit (An in vitro diagnostic medical device (IVD)) (Qualitative histologic stain to selectively indicate Mycobacterium and other acid fast organisms) Lot Numbers: D05755, D11015, E1024 and E03378ARTG Number 174922
  • Manufacturer

Manufacturer