Device Recall CELLTRACKS ANALYZER II 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Veridex, LLC 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
    64304
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-1950-2013
  • 사례 시작날짜
    2012-12-28
  • 사례 출판 날짜
    2013-08-10
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2015-08-11
  • 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
    System, immunomagnetic, circulating cancer cell, enumeration - Product Code NQI
  • 원인
    Veridex, llc has received a report that a patient's demographics were incorrectly associated with another patient's identification (pid) number. the purpose of this notification is to inform you of the issue and provide instructions to help prevent an occurrence on your celltracks autoprep system and celltracks analyzer ii.
  • 조치
    Veridex sent an Important Product Correction Notification letter dated December 28, 2012, to all affected customers. The letter identified the affected product, problem and actions to be taken. Customers were instructed to complete and return the Confirmation of Receipt form. For questions contact Customer Technical Services at 1-800-421-3311.

Device

  • 모델명 / 제조번호(시리얼번호)
    CELLTRACKS ANALYZER II (Software Version 2.5.1 & Below). Product Code: CT1476B (9555).
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Worldwide Distribution - USA Nationwide and the countries of Australia, Canada, China, India, Japan, Singapore, England, France, Germany, Italy and Spain.
  • 제품 설명
    CELLTRACKS ANALYZER II (Software Version 2.5.1 & Below. || Product Usage: || The CELLTRACKS AUTOPREP System is a general purpose laboratory instrument used with immunomagnetic reagents that capture and enrich target cells, and labeling reagents that differentiate cells in whole blood. Cell analyzers such as the CellTracks Analyzer II, CellSpotter System, flow cytometers or microscopes may be used for cell identification and enumeration. The system is fit for in vitro diagnostic use. In the CellTracks Analyzer II software 2.5.1 release notes Pub. No. J40136EN issued 2012-03-26 page 1, the document states that the edit patient sample information screen now includes a patient information section, a new feature unique to software 2.5.1. This section provides a drop down for patient race and cancer type. There are also separate fields for first and last name for both the physician and patient. There is no mention of the drop down patient ID box on the right side of the user interface which auto-populates previous sample data.
  • Manufacturer

Manufacturer

  • 제조사 주소
    Veridex, LLC, 1001 US Route 202, Raritan NJ 08869-0606
  • 제조사 모회사 (2017)
  • Source
    USFDA