Merit 7F Prelude Short Sheath Introducers 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Merit Medical Systems 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
    2017-03-31
  • 사례 출판 날짜
    2017-03-31
  • 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: merit 7f prelude short sheath introducers the united states food and drug administration (fda) has issued a medical device safety alert concerning merit 7f prelude short sheath introducers [lot numbers: h1041469, h1041473, h1036880, h1041464; catalogue numbers: k15-00070, k15-00170, pss-7f-4-035mt, pss-7f-4mt; manufacturing dates: 23 nov 2016 to 30 nov 2016; distribution dates: 15 dec 2016 to 18 jan 2017], manufactured by merit medical systems, inc. the manufacturer is recalling the prelude short sheath introducer due to a manufacturing defect which may cause the tip to separate from the sheath during the insertion procedure. if this occurs, the tip could enter the patient's bloodstream. this may result in prolonged procedure times, additional surgery to remove the tip from the patient, blood clots, internal tears and perforation to arteries or veins, excessive bleeding, and death. the manufacturer advises users to quarantine and discontinue use of the affected products and return them to the manufacturer. for details, please refer to the fda website: https://www.Fda.Gov/medicaldevices/safety/listofrecalls/ucm549795.Htm if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 31 march 2017.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Merit 7F Prelude Short Sheath Introducers
  • Manufacturer

Manufacturer