DiaClon Anti-Lea ID-Card 의 리콜

L’Agence nationale de sécurité du médicament et des produits de santé (ANSM)에 따르면, 해당 리콜 는 France 에서 Diamed 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
    2005-11-15
  • 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
    The DIAMED company has informed the Afssaps of the recall of lots 50241.30.01 (per 30/11/05), 50241.30.02 (per 31/12/05), 50241.30.03 (per 31/01/06) of the DMDIV called DiaClon Anti-Lea ID-Card, reference 007221 and lot 50371.02.01 (per 30/11/05) of the DMDIV called Antigen ID-card profile I, reference 008510 .. These devices are used for the determination of the Lewis antigen has (inter alia, for the Antigen I-profile card I) thanks to monoclonal anti-Lea antibodies included in the gel. This measure follows the demonstration of a weakening of the reactivity of the monoclonal antibodies. anti-Lea .. This information is intended for laboratory managers, directors of health establishments and correspondents for reactive vigilance for dissemination, where appropriate, to the services concerned.

Device

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

Manufacturer

  • Source
    LAANSM