Hudson RCI Pediatric Anaesthesia Breathing Circuits 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Teleflex Medical 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
    2014-10-08
  • 사례 출판 날짜
    2014-10-08
  • 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: teleflex medical hudson rci pediatric anaesthesia breathing circuits the united states food and drug administration (fda) issued a medical device safety alert concerning hudson rci pediatric anaesthesia breathing circuits, manufactured by teleflex medical. the affected products were manufactured from march 2013 to july 2014 and distributed from june 2013 to may 2014. according to the fda, the ends of the devices may crack or break before or during use. this could cause serious health risks, including delayed patient treatment and breathing difficulties if not replaced immediately. use of this device may also cause death. on september 8, 2014, the manufacturer sent customers an urgent medical device recall letter explaining the device problem and actions to be taken. the manufacturer recommends the following actions:- stop using the devices. remove the devices from inventory and stop distribution. for details, please refer to the following fda websites: http://www.Fda.Gov/safety/medwatch/safetyinformation/safetyalertsforhumanmedicalproducts/ucm417868.Htm http://www.Fda.Gov/medicaldevices/safety/listofrecalls/ucm417731.Htm if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 8 october 2014.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 의료기기 분류등급
  • 제품 설명
    Medical Device Safety Alert: Teleflex Medical Hudson RCI Pediatric Anaesthesia Breathing Circuits
  • Manufacturer

Manufacturer