Hydrochloric Acid 6 Molar 30mL Containers. An in vitro diagnostic medical device (IVD) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Thermo Fisher Scientific 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-2018-RN-00489-1
  • 사례 위험등급
    Class III
  • 사례 시작날짜
    2018-05-17
  • 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
    Thermo fisher scientific has identified that the plain container patient information label adhered to specimen jars for specific lots is incorrect as it contains the phrase "10% neutral buffered formalin". the correct label is exactly the same, but without the "10% neutral buffered formalin" phrase. the product information on the box (contains the containers) and content label on the containers are correct.
  • 조치
    Thermo Fisher is advising customers to identify and quarantine affected product. Thermo Fisher will contact users to arrange replacement or credit of stock.

Device

  • 모델명 / 제조번호(시리얼번호)
    Hydrochloric Acid 6 Molar 30mL Containers. An in vitro diagnostic medical device (IVD)Catalogue Number: FNNHCL/30Lot Numbers: 1708249410 and 1803258790ARTG Number: 243713(Thermo Fisher Scientific Australia - Specimen receptacle IVDs)
  • Manufacturer

Manufacturer