VITROS Signal Reagent 의 리콜

L’Agence nationale de sécurité du médicament et des produits de santé (ANSM)에 따르면, 해당 리콜 는 France 에서 Ortho-Clinical Diagnostics 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
    2006-04-05
  • 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
    On April 3, 2006, Ortho-Clinical Diagnostics France withdrew from the market lot 8350 (05/06/2006 expiry) of the in vitro diagnostic medical device called Signal Reagent VITROS reference CAT 107 2693 following the receipt of claims relating to biases observed on the results when using this lot of reagent. This device is used to generate the luminescence signal in all Immunoassay tests on VITROS ECi / ECiQ systems. In addition, the company informs all users of VITROS ECi / ECiQ systems of the need to follow a reinforced quality control procedure for each pack of all lots of VITROS Signal Reagent used, by means of the enclosed message (03/04 / 2006) (275 KB) validated by Afssaps. The European competent authorities concerned are informed directly by the manufacturer. This information is intended for laboratory managers, the directors of health establishments and the reactovigilance correspondents for dissemination, where appropriate, to the services concerned. Alert of 17 July 2006 - update

Device

Manufacturer