Etest COLISTIN CO256 WW 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 BioMerieux 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

안전성 경고는 의료기기 제품과 관련된 중요한 정보와 권고사항을 담고 있습니다. 물론 안전성 경고가 배포되었다고 해서 해당 제품이 무조건 안전하지 않은 제품이라는 것은 아닙니다. 보건의료업계 종사자와 의료기기 사용자들에게 배포되는 안전성 경고에는 회수(recall)도 포함될 수 있습니다. 제조사가 안전성 경고를 작성하기도 하지만, 보건당국에서 작성하는 경우도 있습니다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Safety alert
  • 날짜
    2016-08-02
  • 사례 출판 날짜
    2016-08-02
  • 사례 국가
  • 사례 출처
    DH
  • 사례 출처 URL
  • 비고 / 경고
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), 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 data from the U.S. and Hong Kong.
  • 데이터 추가 비고
    Medical Device Safety Alert
  • 원인
    Medical device safety alert: biomerieux etest colistin co256 ww medical device manufacturer, biomerieux, has issued a field safety notice concerning its etest colistin co256 ww. the affected product reference numbers are 537300 and 537308. based on scientific publications (including eucast warning letter on their website) on colistin gradient and disk diffusion tests, the manufacturer was alerted about a potential underestimation of the minimum inhibitory concentrations (mic) values for enterobacteriaceae and acinetobacter, the manufacturer initiated a complaint investigation to confirm product performance and determine root cause. while the internal and external investigations are still ongoing, to date and based on data available, the following have been identified: the etest colistin co256 performance are depending on the mueller hinton agar plate used as described in the supplement insert (ref.16266, version a)- cis012. for the enterobacteriaceae strains, the first results of the manufacturer’s investigation state that the performance of etest colistin co256 are conformed if used in conjunction with the mhe agar (from the manufacturer) with a good concordance rate compared to broth-micro dilution (bmd) method. there is a potential of false susceptible results on etest colistin co256 ww (ref. 537300-537308) with some mueller hinton agar (except with the mhe agar from the manufacturer for the enterobacteriaceae strains). these data need to be confirmed by the investigations ongoing. the manufacturer requests users to take the following actions: for enterobacteriaceae strains, users can continue to use the affected lots of etest colistin co256 (ref. 537300- 537308) for diagnostic purposes, only if it is used with mh-e (mueller hinton-e agar from the manufacturer’s ref. 413822-413823-413824-413825) agar. if not, or if users test other strains than enterobacteriaceae strains, the manufacturer recommends users to restrict its use to epidemiological surveys. among tests previously performed, identify any possible false susceptible results, analyze the related risks and determine appropriate actions if relevant. according to the local supplier, the affected products are distributed in hong kong. if you are in possession of the products, please contact your supplier for necessary actions. posted on 2 august 2016.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: BioMerieux Etest COLISTIN CO256 WW
  • Manufacturer

Manufacturer