BURETROL Solution Set with 150ml INTERLINK Burette 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
    2014-07-25
  • 사례 출판 날짜
    2014-07-25
  • 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 buretrol solution set with 150ml interlink burette medical device manufacturer, baxter healthcare, has issued a field safety notice (fsn) concerning its buretrol solution set with 150ml interlink burette. the affected product code is 2c7564 with the lot numbers dr13e06019, dr13j24021, dr13j24039 and dr13l11016. the affected products were distributed to customers between 14 march 2014 and 30 june 2014. according to the manufacturer, the voluntary recall was issued due to complaints of separation between the burette chamber and the drip chamber. the root cause for this issue has been identified and resolved. if the separation is not detected before connection with the administration set, there is a risk of contamination of the sterile fluid path which could lead to blood stream infection or sepsis and may be life-threatening. additionally, air may be aspirated into the vascular system, causing venous air embolism, which while is improbable may be life-threatening. there have been no adverse events reported for this issue. according to the local supplier, the affected products were distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 25 july 2014.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Baxter BURETROL Solution Set with 150ml INTERLINK Burette
  • Manufacturer

Manufacturer