Automated Haematology Analyser 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Sysmex 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
    2013-10-16
  • 사례 출판 날짜
    2013-10-16
  • 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: sysmex automated haematology analyser the medicines and healthcare products regulatory agency (mhra), united kingdom (uk) has posted a field safety notice concerning automated haematology analyser [model no: xn-10 & xn-20; serial no.: all], manufactured by sysmex corporation. the manufacturer was informed from the uk market that in very rare cases falsely high haemoglobin (hb) values may occur, creating the potential risk of missed transfusions for patients with low hb values. as this does not occur in samples which were mixed correctly, the manufacturer deduces that correct pre-analytical procedures and mixing can prevent this phenomenon. in studies performed on the xn-series analysers, the manufacturer has confirmed that the mixing function is effective for healthy volunteer samples which are measured less than 4 hours after the blood has been collected. however, for other samples with high viscosity or erythrocyte sedimentation rates (e.G. polymyalgia rheumatica, temporal arteritis or malignant lymphoma) or samples stored in the refrigerator, there is the possibility that the instruments standard mixing cycle may not be sufficient to suitably mix the sample. affected users are reminded to always ensure that samples are mixed sufficiently before being placed on the analyser, especially for samples from patients prone to high degrees of sedimentation or for cooled samples. according to the local supplier, the affected products were distributed in hong kong. for details, please visit the following mhra website: http://www.Mhra.Gov.Uk/safetyinformation/safetywarningsalertsandrecalls/fieldsafetynotices/con321967 if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 16 october 2013.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Sysmex Automated Haematology Analyser
  • Manufacturer

Manufacturer