MARS Kit Gambro, Type 1116/1-X-MARS 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Baxter Healthcare 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
    2018-01-03
  • 사례 출판 날짜
    2018-01-03
  • 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: baxter healthcare mars kit gambro, type 1116/1-x-mars medical device manufacturer, baxter healthcare, has issued a medical device safety alert concerning its mars kit gambro, type 1116/1-x-mars [product code: 800540; lot numbers (expiration date): 22651 (01 september 2019), 22708 (30 september 2019)]. the manufacturer has received customer complaints regarding leakage in the albumin circuit. the leakage was caused by an inadequate adhesive connection of the tubing to the hansen connector of the mars tube set which is part of the mars treatment kit. according to the manufacturer, an undetected leaking albumin circuit could lead to excessive fluid removal from the patient during albumin dialysis. this could lead to hypovolemia. delay or interruption of therapy may also occur if the issue is detected during priming. the manufacturer has not received any reports of adverse events or patient injury associated with this issue. affected users are advised to locate and remove all affected product from facility. product recall is on-going. according to the local supplier, the affected products are distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 03 january 2018.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Baxter Healthcare MARS Kit Gambro, Type 1116/1-X-MARS
  • Manufacturer

Manufacturer