Device Recall Agendia MammaPrint 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Agendia Inc 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
    54930
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-1321-2010
  • 사례 시작날짜
    2010-03-03
  • 사례 출판 날짜
    2010-04-12
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2010-06-18
  • 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
    Classifier, prognostic, recurrence risk assessment, RNA a gene expression, breast cancer - Product Code NYI
  • 원인
    Over a period of about 6 months in about 15% of results provided agendia has been "over reporting" the chance of metastasis risk being 29% risk of recurrence instead of 10% risk. this over reporting of risk did not cause direct injury to patients. however, if used by physicians as the sole basis for decision-making, affected patients may have received unnecessary therapy.
  • 조치
    Communication with physicians was initiated by the firm's Chief Medical Officer on March 3, 2010. The firm's representatives will meet with treating physicians in person while having the corrected results in hand to inform each in person of the action, to allow a decision of the best course of action. Physicians will be provided with background information on the issue at hand and corrected results. As follow up, the physician would receive a corrected report per patient by FedEx in order to register the reception of corrected information. Because each user received a personal visit, no other contact information was planned or provided by Agendia.

Device

  • 모델명 / 제조번호(시리얼번호)
    MP US version 03
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Nationwide.
  • 제품 설명
    Agendia MammaPrint, Catalog Numbers MP01, MP US version 03
  • Manufacturer

Manufacturer

  • 제조사 주소
    Agendia Inc, 17742 Beach Blvd Ste 250, Huntington Beach CA 92647-6835
  • 제조사 모회사 (2017)
  • Source
    USFDA