REAGENT KIT hsCRP VITROS, Model HsCRP Reagent Kit Cx 6 / 50T - Registro 80145900837 - Lote 28-3487 의 안전성 경고

Agência Nacional de Vigilância Sanitária (ANVISA)에 따르면, 해당 안전성 경고 는 Brazil 에서 Johnson & Johnson do Brasil Ind. e Com. de Prod. para Saúde Ltda 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
  • 사례 ID
    1391
  • 날짜
    2014-05-14
  • 사례 국가
  • 사례 출처
    ANVISA
  • 사례 출처 URL
  • 비고 / 경고
    Brazilian data is current through June 2018. All of the data comes from Anvisa, 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 Brazil.
  • 데이터 추가 비고
    The company informs that European Reference Material (ERM) is a calibration reference standard used to support the assigned value of the calibrator kit VITROS® 17 and VITROS® FS Calibrator 1. Both calibrators are used together to calibrate the calibration systems. VITROS® 5,1 FS, VITROS®4600 and VITROS®5600 integrated systems for quantitative measurement of Reactive Protein C (CRP) using the VITROS hsCRP reagent. CRP is used to assess the risk of developing coronary heart disease (CHD). The risk of coronary heart disease increases with CRP values ​​greater than 3 mg / L. The client should discuss any concerns they may have about the results reported previously with their medical director or the requesting physician. The results from this or any other diagnostic test should be used and interpreted only in the context of the entire clinical picture #### UPDATED ON 08/18/2017, the field action documentations submitted by the company are filed in the area. If necessary, the area can reassess the field action at any time.
  • 원인
    This product correction was initiated because the calibrator values ​​assigned to the batches of listed calibrator kits were released through a reference method, which was subjected to validation of a new batch of european reference material (erm). the validation process was not completed before the calibrator value for vitros ® hscrp reagent (product code 6801739), generation (gen) 28. the manufacturer identified this event internally, and there were no reports of customer complaints related to the subject.
  • 조치
    The company urges customers to - Immediately discontinue use of the VITROS hsCRP, GEN28 reagent until the installation of ADD 5784 or above. - Install ADD 5784 on your VITROS® System as soon as you receive it. After a successful recalibration, the remaining VITROS ® hsCRP, GEN 28 Reagent in the inventory may be used

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