EnVision + 의 리콜

L’Agence nationale de sécurité du médicament et des produits de santé (ANSM)에 따르면, 해당 리콜 는 France 에서 DakoCytomation 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
  • 날짜
    2005-10-27
  • 사례 국가
  • 사례 출처
    ANSM
  • 사례 출처 URL
  • 비고 / 경고
    French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), 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 France.
  • 데이터 추가 비고
  • 조치
    In agreement with Afssaps, the company DakoCytomation removed from the market the references and lots (27/10/2005) (155 Kb) cited in the appendix of the in vitro diagnostic medical device called EnVision +. This measure follows the discovery of an error in the formulation of the system of visualization kits of references and batches mentioned above, which may cause a slight decrease in the signal strength on some samples .. This device is used with mouse or rabbit primary antibodies provided by the user, for the qualitative identification of antigens by light microscopy in paraffin-embedded normal and pathological tissues, sections of tissue cryostats or cell preparations. The company has warned directly the recipients of the references / batches incriminated by means of the attached message (27/10/2005) (11 ko) validated by the Afssaps .. The European competent authorities concerned are informed directly by the manufacturer .. This information s address to laboratory managers, health facility directors and health-vigilance correspondents for dissemination, where appropriate appropriate to the services concerned.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    in-vitro_medical_device
  • Manufacturer

Manufacturer

  • Source
    LAANSM