Device Recall Perkin Elmer 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Perkinelmer 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
    72808
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-0632-2016
  • 사례 시작날짜
    2015-12-08
  • 사례 출판 날짜
    2016-01-12
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2017-08-04
  • 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
    Counter (beta, gamma) for clinical use - Product Code JJJ
  • 원인
    The content of the second #023 barcode id label in the barcode id label binder is incorrect. the second barcode id label #023 symbol incorrectly identifies as #024 when scanned. if measurement protocols have been programmed for both id #023 and #024, the protocol associated with barcode id #024 is executed. if the error is undetected, the gamma counter may produce erroneous results.
  • 조치
    Perkin Elmer sent an Urgent Medical Device Correction letter dated December 7, 2015 to affected customers. The letter identified the affected products, problems and actions to be taken. Customers were instructed to destroy all affected products in their possession. Customers were asked to complete the enclosed Correction Response Form and return it by scan and e-mail to QMresponse.SG@perkinelmer.com . Corrected barcode labels ID #023 will be provided upon request and return of the completed Correction Response Form to PerkinElmer. For further information contact your local PerkinElmer representatives..

Device

  • 모델명 / 제조번호(시리얼번호)
    Serial Numbers: DG06106539 DG12118720 DG07106646 DG12107250 DG12107281 DG03117619 DG11118605 DG01117400 DG12107202 DG01117401 DG06106449 DG03117666 DG05117791 DG06106454 DG03106180 DG11118637 DG07118121 DG07106598 DG11118633 DG06106520 DG03106137 DG07118111 DG02128888 DG08118247 DG06118014 DG01128790 DG12107207 DG07106637 DG01128876 DG04117764 DG01106035 DG12118780 DG05106342 DG01117399 DG06117909 DG06118011 DG09106846 DG11107146 DG12118694 DG08118217 DG02106084 DG04117690 DG05117838 DG09106799 DG04117735 DG03117548 DG01117362
  • 의료기기 분류등급
  • 의료기기 등급
    1
  • 이식된 장치?
    No
  • 유통
    Worldwide Distribution - US Nationwide and the countries of ARGENTINA, AUSTRALIA, AUSTRIA, BELGIUM, BOLIVIA, BRAZIL, CANADA, CHINA, DENMARK, FINLAND, FRANCE, GERMANY, GREAT BRITAIN, GREECE, HONG KONG, INDIA, IRELAND, ISRAEL, ITALY, JAPAN, KOREA, KUWAIT, MYANMAR, NETHERLANDS, NEW ZEALAND, NORWAY, POLAND, PORTUGAL, SAUDI ARABIA, SINGAPORE, SLOVAKIA, SOUTH AFRICA, SPAIN, SWEDEN, SWITZERLAND, TAIWAN, and THAILAND.
  • 제품 설명
    Perkin Elmer WIZARD2 1-detector, 550 samples Product Code: 2470-0010 || The Wizard gamma counter is intended to detect and count gamma radiation emitted by clinical samples
  • Manufacturer

Manufacturer

  • 제조사 주소
    Perkinelmer, 940 Winter Street, Waltham MA 02451
  • 제조사 모회사 (2017)
  • Source
    USFDA