Device Recall UniCel DxI 800 Access Immunoassay Systems 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Beckman Coulter 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
    57952
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-1938-2011
  • 사례 시작날짜
    2011-01-26
  • 사례 출판 날짜
    2011-04-11
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2012-06-04
  • 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
    Analyzer chemistry (photometric, discrete), for clinical use - Product Code JJE
  • 원인
    The recall was initiated due to beckman coulter receiving a report of results that were associated with incorrect patient identifications when two sample racks advanced into the sample presentation area in one push. the first rack of the two was not scanned. this is referred to as a "pushed pair." if a pushed pair event occurs, results may be associated with the incorrect patient identification.
  • 조치
    Beckman Coulter sent an Urgent: Field Safety Notice Product Correction letter dated January 26, 2011, via US Postal Service to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to: 1. To prevent a pushed pair, be sure your sample racks are free of debris prior to use. Do not apply additional labels to the sample racks. Extra labels can obscure the edges of a sample rack, or obstruct the gap between two racks. Be sure sample labels do not extend beyond the edges of a sample rack; 2. If a pushed pair occurs on the UniCel DxI system, the system generates a yellow Event Log message - Clear the presentation tray and press ROUTINE button. This Event Log message is associated with a variety of common Sample Presentation Unit (SPU) errors. For that reason, you must review the Event Log details to confirm the pushed pair event has not occurred; 3. Detach the Appendix included with this notification and store it near your UniCel DxI system. Use the Appendix as a reference if you suspect a pushed pair event has occurred on your system. Beckman Coulter also requested their customers share the recall information with their laboratory staff, and retain pages 1 and 2 of this notification as part of your laboratory Quality System documentation. For questions regarding ththe recall notification, customers were instructed to contact Beckman Coulter Customer Support Center on the Beckman Coulter website at http://www.beckmancoulter.com/customersupport/support, or call 1-800-854-3633 in the United States or Canada. Outside the United States and Canada, contact their local Beckman Coulter Representative.

Device

  • 모델명 / 제조번호(시리얼번호)
    DxI System Software versions: 2.3, 2.4, 4.1, 4.2.1, 4.3 (Current released version), 4.3.2 (Released to a single Japanese customer only)
  • 의료기기 분류등급
  • 의료기기 등급
    1
  • 이식된 장치?
    No
  • 유통
    Worldwide Distribution - USA (nationwide) and the countries of Algeria, Angola, Australia, Austria, Belgium, Brazil, Bulgaria, Canada, China, Colombia, Croatia, Czech Republic, Denmark, Finland, France, French Polynesia, Germany, Greece, Hong Kong, Hungary, India, Ireland, Israel, Italy, Japan, Jordan, Republic of Korea, Kuwait, Liechtenstein, Malaysia, Mayotte, Mexico, Morocco, Namibia, Netherlands, New Zealand, Norway, Philippines, Poland, Puerto Rico, Romania, Russian Federation, Singapore, Slovakia, South Africa, Spain, Swaziland, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, United Arab Emirates, United Kingdom, Venezuela, and Vietnam.
  • 제품 설명
    UniCel DxI 800 Access Immunoassay || Systems; Part Number(s): DxI 800: 973100, DxI 800 Remanufactured || A25288, DxI 800 with spot B A71456, DxI 800 || Reconditioned A25285 || The DxI Immunoassay System is an in vitro diagnostic device used for the quantitative, semi-quantitative or qualitative determination of various analyte concentrations found in human body fluids.
  • Manufacturer

Manufacturer

  • 제조사 주소
    Beckman Coulter Inc., 200 S Kraemer Blvd, Brea CA 92821-6208
  • 제조사 모회사 (2017)
  • Source
    USFDA