Bloodlines in used with Integra and AK machines 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Gambro 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
    2013-01-29
  • 사례 출판 날짜
    2013-01-29
  • 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: gambro bloodlines in used with integra and ak machines the medicines and healthcare products regulatory agency (mhra), united kingdom posted a field safety notice concerning bloodlines, manufactured by gambro. the affected devices are identified by the following product codes: 114626, 114562, 114525, 114620, 114526, 114527, 114524, 114563, 114635, 114557, 114561, 114636, 114651, 114625, and 11462. the manufacturer has identified a potential for increased likelihood of clotting following the introduction of the new venous chamber on conventional bloodlines which are used with the integra and ak machines. the new venous chamber design may increase the likelihood of clotting due to the presence of potentially stagnant areas beside the blood flow inlet. the manufacturer has intended to re-introduce the original venous chamber in the gambro bloodlines. the re-introduction of the original design will start from the beginning of march 2013. in the interim, the manufacturer is providing additional instructions for the correct blood level setting in the new venous chamber. the manufacturer has established from reported incidents, that the potential for clotting is influenced by the blood level in the venous chamber and anticoagulant regime. the manufacturer would like to emphasize the need for anticoagulants must be determined for the specific patient by the attending physician. for details, please refer to mhra website http://www.Mhra.Gov.Uk/safetyinformation/safetywarningsalertsandrecalls/ fieldsafetynotices/con226926 if you are in possession of the product, please contact your supplier for necessary actions. posted on 29 january 2013.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Gambro Bloodlines in used with Integra and AK machines
  • Manufacturer

Manufacturer