Merifluor EBV VCA IgM IFA (an Immunofluorescence Test for the Detection of Antibodies). An in vitro diagnostic medical device (IVD) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Bioline Aust 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-00167-1
  • 사례 위험등급
    Class III
  • 사례 시작날짜
    2016-02-11
  • 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
    A report has been received that the foil pouches for some ebv-na substrate slides appear to have been damaged, resulting in exposure to moisture and a decrease in slide reactivity/loss of fluorescence. it has also been determined that the desiccant packaged with the compromised ebv-na substrate slides have turned pink, indicating exposure to moisture. the desiccants are typically blue. internal testing has demonstrated that the positive control tested with an ebv-na substrate slide from a damaged pouch with pink desiccant shows no fluorescence, which is interpreted as an invalid reaction according to the product package insert. there is no impact to patients. this action was carried out prior to consultation with the therapeutic goods administration (tga).
  • 조치
    Bioline is advising users to check the colour of the desiccant prior to use. If the desiccant is pink, the slides should not be used. Blue desiccant pouches can be used to testing if the control results are acceptable. This action has been closed-out on 03/08/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    Merifluor EBV VCA IgM IFA (an Immunofluorescence Test for the Detection of Antibodies). An in vitro diagnostic medical device (IVD)Lot Number: EB150G160Substrate Slide Lot Number: 2921-366Expiry Date: 30 June 2016ARTG Number: 214645
  • Manufacturer

Manufacturer