Arterial Venous Fistula (AVF) sets for Haemodialysis - Safety AVF Needle fixed wing 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Kawasumi Laboratories Inc 에 의해 제조된 제품과 관련되어 있습니다.

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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
    2015-11-26
  • 사례 출판 날짜
    2015-11-26
  • 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: kawasumi laboratories inc. arterial venous fistula (avf) sets for haemodialysis - safety avf needle fixed wing the therapeutic goods administration (tga) of australia has posted a medical device safety alert concerning the arterial venous fistula (avf) sets for haemodialysis - safety avf needle fixed wing manufactured by kawasumi laboratories inc. the affected catalogue numbers are avfe1525clfg and avfe1525cplfg and the affected lot numbers include 140714i8, 141014i5, 141110i1, 150128i7, 150511i1, 140912i6, 141110i2. the manufacturer has received four reports worldwide where the needle cannula of the arterial venous fistula set for haemodialysis had separated from the needle hub and remained in the patient’s vein when attempting to remove the needle following the completion of the dialysis treatment. although the possibility of occurrence for such an event is extremely low, there is potential that blood leakage could occur should the needle cannula separate from the hub and remain in the patient’s vein. there have been no reports of patient injury as a result of this issue. the manufacturer advises users to stop using the affected products from the affected population. customers are advised to quarantine and destroy all affected products in the affected population. for details, please refer to the tga website: http://apps.Tga.Gov.Au/prod/sara/arn-detail.Aspx?k=rc-2015-rn-01147-1 if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 26 november 2015.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Kawasumi Laboratories Inc. Arterial Venous Fistula (AVF) sets for Haemodialysis - Safety AVF Needle fixed wing
  • Manufacturer

Manufacturer