Device Recall BD FMC7 FITC 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Becton, Dickinson and Company, BD Biosciences 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
  • 사례 ID
    72885
  • 사례 위험등급
    Class 3
  • 사례 연번
    Z-0628-2016
  • 사례 시작날짜
    2015-12-14
  • 사례 출판 날짜
    2016-01-11
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2016-10-31
  • 사례 출처
    USFDA
  • 사례 출처 URL
  • 비고 / 경고
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • 데이터 추가 비고
    Reagents,specific,analyte - Product Code MVU
  • 원인
    Becton, dickinson and company (bd) has determined that the fmc7 fitc (asr) is exhibiting functional degradation. the functional degradation has the effect of reducing the percent positive from 100% down to approximately 87%.
  • 조치
    BD Biosciences sent an Urgent Product Recall letter dated December 2015, to all affected customers to inform them that Becton, Dickinson and Company (BD) has determined that the FMC7 FITC (ASR) is exhibiting functional degradation. The letter informs the customers of the problems identified and the actions to be taken. Customers are instructed to return the Tracking/Verification form to BD Biosciences. Customers are instructed to contact BD Customer Support at (877) 232-8995 (prompt 3, 3) in the US. Customers outside of the US are instructed to contact their local BD Biosciences or distributor.

Device

Manufacturer

  • 제조사 주소
    Becton, Dickinson and Company, BD Biosciences, 2350 Qume Dr, San Jose CA 95131-1812
  • 제조사 모회사 (2017)
  • Source
    USFDA