ortho biovue system cassettes 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Ortho Clinical Diagnostics 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
    2013-07-09
  • 사례 출판 날짜
    2013-07-09
  • 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: ortho clinical diagnosticsortho biovue system cassettes the medicines and healthcare products regulatory agency(mhra), united kingdom posted a field safety notice concerningortho biovue system cassettes, manufactured by ortho clinical diagnostics. ortho clinical diagnostics has identified isolated occurrences of improperly positioned cassette labels for certain products.An investigation confirmed that the cause of the issue occurred on one of our three manufacturing lines following a particular sequence of events.The occurrence rate of the issue is very low. the use of an affected multi-reagent cassette may lead to false negative or false positive results causing a potential misclassification of the patient or donor blood groups or incorrect antibody detection results. there is no risk associated with the use of an affected single-reagent cassette since all wells contain the same reagent. the manufacturer advises users to inspect all cassettes from the potentially affected lots remaining in facility prior to use, by referring to the ortho biovue system cassette inspection procedure for visual detailed instructions; and do not use cassettes with an incorrectly positioned label and discard the affected cassette in accordance with local regulations. according to the local supplier, the affected products were distributed in hong kong. for details, please refer to mhra website http://www.Mhra.Gov.Uk/safetyinformation/safetywarningsalertsandrecalls/fieldsafetynotices/con287036 if you are in possession of the product, please contact your supplier for necessary actions. posted on 9 july 2013.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Ortho Clinical DiagnosticsORTHO BioVue System Cassettes
  • Manufacturer

Manufacturer