Device Recall diaDexus PLAC Test Reagent Kit 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 DiaDexus, 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
    50482
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-1204-2009
  • 사례 시작날짜
    2008-11-04
  • 사례 출판 날짜
    2009-04-01
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2009-12-21
  • 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
    Lipoprotein-associated phospholipase a2 Immunoassay Test System - Product Code NOE
  • 원인
    Storage equipment failure at distributor site due to hurricane ike caused product to experience a temperature variation and go out of range. the integrity of the product could not be assured.
  • 조치
    The firm and its distributor contacted the consignees via phone on 11/04/08. The firm informed them of the issue and inquired about the products' status. An Urgent: Device Recall letter was issued on 11/04/08 via FedEx. The letter requested that use of the kit be immediately discontinued and returned promptly. A phone call was made to follow up requesting return of the product.

Device

  • 모델명 / 제조번호(시리얼번호)
    sub lot of lot 088061, expiration date 2008-12
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Nationwide Distribution
  • 제품 설명
    diaDexus Inc. PLAC Test Reagent Kit, Turbidimetric Immunoassay for the Quantitative Determination of Lp-PLA2 in Human Plasma or Serum, liquid ready-to-use two-reagent kit assembled in a kit box, manufactured by diaDexus Inc, South San Francisco, CA 94080, Catalog number 90110 || Turbidimetric Immunoassay for the Quantitative Determination of Lp-PLA2 in Human Plasma or Serum on automated clinical chemistry analyzers, to be used in conjunction with clinical evaluations and patient risk assessment as an aide in predicting risk for coronary heart disease, and ischemic stroke associated with atherosclerosis.
  • Manufacturer

Manufacturer

  • 제조사 주소
    DiaDexus, Inc, 343 Oyster Point Blvd, South San Francisco CA 94080
  • 제조사 모회사 (2017)
  • Source
    USFDA