Device Recall Hologic Panther(R) Fusion(TM) 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Hologic, 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
    79007
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-0595-2018
  • 사례 시작날짜
    2018-01-20
  • 사례 상황
    Open, Classified
  • 사례 국가
  • 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
    Instrumentation for clinical multiplex test systems - Product Code NSU
  • 원인
    The panther or the panther fusion glass panel separates from the 19 inch touch screen monitor and could potentially fall and hit an operator.
  • 조치
    The firm sent an Urgent Medical Device Recall Notification dated January 8, 2018 to their customers. The letter identified the affected product, problem and actions to be taken. Customers were instructed that a Hologic representative will contact your site to arrange a visit in order to provide an interim solution to secure the glass panel until a replacement monitor with the issue corrected can be installed. For questions contact Hologic Technical Support. at +1-888-484-4747 or +1-858-410-8511 or by e-mail at molecularsupport@hologic.com

Device

  • 모델명 / 제조번호(시리얼번호)
    Serial Numbers: 2090002307, 2090002308, 2090002309, 2090002310, 2090002311, 2090002312, 2090002339, 2090002340, 2090002341, 2090002342, 2090002343, 2090002344, 2090002345, 2090002346, 2090002347, 2090002348, 2090002349, 2090002350, 2090002351, 2090002352, 2090002353, 2090002359, 2090002360, 2090002361, 2090002362, 2090002363, 2090002366, 2090002367, 2090002368, 2090002369, 2090002370, 2090002371, 2090002372, 2090002373, 2090002374, 2090002381, 2090002382, 2090002383, 2090002384, 2090002385, 2090002387, 2090002388, 2090002389, 2090002390, 2090002391, 2090002393, 2090002404, 2090002405, 2090002406, 2090002407, 2090002409, 2090002411, 2090002413, 2090002414, 2090002415, 2090002420, 2090002421, 2090002422, 2090002428, 2090002429, 2090002430, 2090002432, 2090002433, 2090002434, 2090002435, 2090002436, 2090002437, 2090002438, 2090002446, 2090002447, 2090002448, 2090002449, 2090002450, 2090002451, 2090002452, 2090002458, 2090002462, 2090002465, 2090002466, 2090002467, 2090002468, 2090002469, 2090002470, 2090002471, 2090002472, 2090002473, 2090002476, 2090002481, 2090002483, 2090002484, 2090002485, 2090002338, 2090002394, 2090002417, 2090002431, 2090002463, 2090002464, 2090002492, 2090002491, 2090002490, 2090002489, 2090002488
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Worldwide distribution
  • 제품 설명
    Hologic Panther(R) Fusion(TM), Catalog number ASY-09600 || Product Usage: || The Panther instrument is a fully automated sample-to-result instrument, eliminating the need for batch processing and automates all aspects of nucleic acid testing on a single, integrated platform. The Panther can be test samples with random access or batch managed; can perform multiple assays on the same patient sample with up to 4 different assays simultaneously.
  • Manufacturer

Manufacturer

  • 제조사 주소
    Hologic, Inc, 10210 Genetic Center Dr, San Diego CA 92121-4362
  • 제조사 모회사 (2017)
  • Source
    USFDA