Corporation Citrate Activated Partial Thromboplastin Time (APTT) Cuvettes 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 International Technidyne Corporation 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

안전성 경고는 의료기기 제품과 관련된 중요한 정보와 권고사항을 담고 있습니다. 물론 안전성 경고가 배포되었다고 해서 해당 제품이 무조건 안전하지 않은 제품이라는 것은 아닙니다. 보건의료업계 종사자와 의료기기 사용자들에게 배포되는 안전성 경고에는 회수(recall)도 포함될 수 있습니다. 제조사가 안전성 경고를 작성하기도 하지만, 보건당국에서 작성하는 경우도 있습니다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Safety alert
  • 날짜
    2014-01-03
  • 사례 출판 날짜
    2014-01-03
  • 사례 국가
  • 사례 출처
    DH
  • 사례 출처 URL
  • 비고 / 경고
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Hong Kong.
  • 데이터 추가 비고
    Medical Device Safety Alert
  • 원인
    Medical device safety alert: international technidyne corporation citrate activated partial thromboplastin time (aptt) cuvettes the australia therapeutic goods administration (tga) posted a medical device safety alert concerning citrate activated partial thromboplastin time (aptt) cuvettes manufactured by international technidyne corporation.The affected lot numbers are e3jcc013-p1 and e3jcc014-p2 and the expiration date is may 2014. the manufacturer has determined that citrate aptt cuvettes from the lots listed above may recover higher than expected results in normal individuals. the manufacturer's investigation into the affected lots identified that when performing tests on non-heparinized e.G., normal blood samples, results may average higher than historic values. test results performed on patients receiving heparin therapy are not affected. the manufacturer has evaluated the risk to health using the affected device and has determined under a variety of clinical conditions, an erroneous increase in the citrated aptt baseline may contribute to serious injury. customers are requested to inspect their stock and quarantine all affected lots of the product, which will be arranged for recovery and replacement. customers are also advised to discuss with the laboratory director about the requirement for retesting of reported patient results. for details, please visit the following tga website: http://www.Tga.Gov.Au/sara/arn-detail.Aspx?k=rc-2013-rn-01364-1 if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 3 january 2014.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: International Technidyne Corporation Citrate Activated Partial Thromboplastin Time (APTT) Cuvettes
  • Manufacturer

Manufacturer