Events

Device Recall FACTOR II (PROTHROMBIN) G20210A Kit, LightCycler 2.0 Instrument 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Roche Molecular Systems, 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
    53708
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z1006-2010
  • 사례 시작날짜
    2009-03-12
  • 사례 출판 날짜
    2010-03-05
  • 사례 상황
    Terminated
  • 사례 국가
    United States
  • 사례 종료 날짜
    2010-06-09
  • 사례 출처
    USFDA
  • 사례 출처 URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=86392
  • 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
    Test, factor ii g202 10a mutations, genomic dna pcr - Product Code NPR
  • 원인
    Within the precautions and warning section, polymorphism heading, of the product's package insert, it stated that mutations at positions 20207, 20209, 20218 and 20221 exist and these mutations are spanned by the mutation probe. these rare mutations will lead to an unknown result after performing genotyping.
  • 조치
    Product Advisory Notices were sent via e-mail on 3/12/09 to Roche Local Safety Officers and Roche county General Manager. Local Safety Officers and General Managers were to communicate to the end users with the Important Product Notice. In addition, Reagent Bulletin 09-052, dated 3/27/09, was issued to Roche U.S. Affiliate of U.S. customers.

Device

Device Recall FACTOR II (PROTHROMBIN) G20210A Kit, LightCycler 2.0 Instrument
  • 모델명 / 제조번호(시리얼번호)
    All lots between 12/18/03 and 4/16/09.
  • 의료기기 분류등급
    Hematology and Pathology Devices
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Nationwide Distribution
  • 제품 설명
    FACTOR II (PROTHROMBIN) G20210A Kit, LightCycler 2.0 Instrument. Material Number 03610195 001 || Cont. || 1 FIIG20210A MD Mix, 1 x 78 uL || 2. FIIG20210A R mix, 1 x 78 uL || 3. FIIG20210A CT, 1 x 50 uL || 5, FIIG20210A DIL 1 x 1 mL || Manufactured in Germany || Distributed by Roche Diagnostics, Indianapolis, IN
  • Manufacturer
    Roche Molecular Systems, Inc.

Manufacturer

Roche Molecular Systems, Inc.
  • 제조사 주소
    Roche Molecular Systems, Inc., 1080 Us Highway 202 S, Somerville NJ 08876-3733
  • 제조사 모회사 (2017)
    Roche Holding AG
  • Source
    USFDA