Yumizen H500 CT (Closed Tube) (Version 2.1.0 or lower) 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 HORIBA ABX SAS 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
    2017-07-11
  • 사례 출판 날짜
    2017-07-11
  • 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: horiba abx sas yumizen h500 ct (closed tube) (version 2.1.0 or lower) the medicines and healthcare products regulatory agency (mhra) of the united kingdom has posted a medical device safety alert concerning yumizen h500 ct (closed tube) (version 2.1.0 or lower), manufactured by horiba abx sas. product development activities by the manufacturer have shown that a defective positioning of the sampling needle could, in some instances, lead to a wear of the rinsing header ring of the needle. this technical issue could generate an over estimation of platelet counting. this background is usually detected when a blank cycle is performed at instrument start up (failed start up alarm). however, in other cases, the blank cycle does not detect the potential abnormal platelet background and could generate erroneous value of platelet counting. the potential overestimation of the platelet counting value could be critical for patients with thrombocytopenia and notably with severe thrombocytopenia which could then not be detected as severe. a corrective action has been identified by the manufacturer which consists of: new sampling needle adjustment needle ring replacement the manufacturer’s technician will implement the corrective action on affected yumizen h500 ct analyzer. while waiting for the corrective action, the manufacturer recommends the following solution for the patient samples with low platelet value suspicion: perform a blank cycle if blank cycle failed, re-run blank cycle if blank cycle passed, re-run their patient sample compare the 2 sample run values and repeat the procedure in case of significant discrepancy. for details, please refer to the mhra’s website: https://www.Gov.Uk/drug-device-alerts/field-safety-notice-3-to-7-july-2017 if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 11 july 2017.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: HORIBA ABX SAS Yumizen H500 CT (Closed Tube) (Version 2.1.0 or lower)
  • Manufacturer

Manufacturer