Events

Columbia Agar ANC + 5% sheep blood 의 리콜

L’Agence nationale de sécurité du médicament et des produits de santé (ANSM)에 따르면, 해당 리콜 는 France 에서 BIOMERIEUX 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
    France
  • 사례 출처
    ANSM
  • 사례 출처 URL
    https://ansm.sante.fr/S-informer/Informations-de-securite-Retraits-de-lots-et-de-produits/retrait-d-une-partie-d-un-lot-du-dmdiv-gelose-columbia-anc-5-de-sang-de-mouton-biomerieux
  • 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 November 10, 2005, the company bioMérieux removed from the market part of lot 798057301 (per 7/12/2005) produced between 3:43 pm and 7:38 pm of the in vitro diagnostic medical device called Columbia Agar ANC + 5% sheep blood reference 43071. This device is a selective isolation medium for the development of Gram (+) bacteria commonly found in clinical specimens. This measurement results from possible growth inhibitions due to the contamination of the part of the lot with a substance inhibiting certain strains of Staphylococcus and certain strains of Listeria. The production time appears legibly on each petri dish, with the other mentions (type of agar, number of batch, etc ..) .. The company directly warned the recipients of the incriminated batch by means of the attached message (10/11/2005) (14 ko) validated by the Afssaps. The European Competent Authorities concerned are informed directly by the manufacturer. This information is intended for laboratory managers, health facility directors and reactive vigilance correspondents for dissemination, where appropriate, to the services concerned.

Device

Columbia Agar ANC + 5% sheep blood
  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    in-vitro_medical_device
  • Manufacturer
    BIOMERIEUX

Manufacturer

BIOMERIEUX