Sunquest Laboratory SMART & Sunquest Laboratory SMART Select 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Sunquest Information 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
    62344
  • 사례 위험등급
    Class 3
  • 사례 연번
    Z-2216-2012
  • 사례 시작날짜
    2011-04-28
  • 사례 출판 날짜
    2012-08-16
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2012-09-04
  • 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
    Calculator/data processing module, for clinical use - Product Code JQP
  • 원인
    In online entry (oex) there are two scenarios where a test result from one container may file to a test on another container. in order for this to occur: 1) site parameter sit 1,2,1,26 (3,217) [restrict resulting of tests to owner container (/n)]=y. 2) the tests are ordered on the same accession number and 3) the test codes are defined to have the same upload code as either replicate or.
  • 조치
    Sunquest sent an Urgent Product Safety Notice dated April 27, 2011, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. For the 103 sites that still have this issue Sunquest distribute a new maintenance release. Customers were instructed to use LabAccess Results Workstation (LARS) instead of Online Entry when entering results for instrument method codes that are defined to use replicate tests that are typically ordered on the same accession. Customers were also instructed to share this notification with appropriate laboratory personnel. Customers were questions should call 520-570-2000. For questions regarding this recall call 520-570-2252.

Device

Manufacturer

  • 제조사 주소
    Sunquest Information Systems, Inc., 250 S Williams Blvd, Tucson AZ 85711-4472
  • 제조사 모회사 (2017)
  • Source
    USFDA