Single Needle Bloodlines for 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
    2014-03-18
  • 사례 출판 날짜
    2014-03-18
  • 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 single needle bloodlines for ak machines the medicines and healthcare products regulatory agency (mhra), united kingdom posted a field safety notice concerning single needle bloodlines for ak machines, manufactured by gambro. the affected product codes (with batch numbers) are 114524 (batch number: from 1317 to 1350), 114561 (batch number: from 1316 to 1401) and 114527 (batch number: from 1316 to 1321) respectively. according to the manufacturer, there is a possible defect on the concerned products, involving a potential bonding of the venous male luer with the drain bag connector and/or of the arterial male luer with the spike connector. when the defect occurs, the cone of the luer may be damaged if the operator forces the disconnection of the bonded luer. performing a treatment with a damaged luer connection could result in an intake of air into the bloodline which could potentially reach the patient and would not pass through the “air in blood” protective system of the dialysis machine. the manufacturer advises users not to use the affected products, but, instead, use product from different lots or similar product as available. the affected product will be collected and replaced by the manufacturer. for details, please refer to the following link:http://www.Mhra.Gov.Uk/safetyinformation/safetywarningsalertsandrecalls/fieldsafetynotices/con391268 if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 18 march 2014.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Gambro Single Needle Bloodlines for AK Machines
  • Manufacturer

Manufacturer