Sarns Soft-Flow Aortic Cannulae and Sarns Venous Return Cannulae 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Terumo Cardiovascular Systems Corporation 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
    2013-10-24
  • 사례 출판 날짜
    2013-10-24
  • 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: terumo sarns soft-flow aortic cannulae and sarns venous return cannulae medical device manufacturer, terumo cardiovascular systems corporation (terumo cvs), has issued a field safety notice concerning sarns soft-flow aortic cannulae and sarns venous return cannulae. the details of the affected products are as follows: sarns soft-flow aortic cannulae without suture flange, angled tip, wire-reinforced with luer port, aortic cannula, 8.0 mm (24 fr) od with 3/8” connector, 14” (36 cm) long : catalogue number 5762, lot number 0677300, and date of distribution from 2 august 2012 through 7 august 2012 sarns soft-flow aortic cannulae without suture flange, straight tip, wire-reinforced with luer port, aortic cannula, 7.0 mm (21 fr) od with 3/8” connector, 14” (36 cm) long: catalogue number 5798, lot number 0677301 and date of distribution from 13 september 2012 through 17 september 2012 sarns soft-flow aortic cannulae without suture flange, straight tip, wire-reinforced with luer port, aortic cannula, 8.0 mm (24 fr) od with 3/8” connector, 14” (36 cm) long: catalogue number 5841, lot number 0677302, and date of distribution from 26 october 2012 through 14 february 2013 sarns venous return cannulae, 20 fr with 1/4” flare, 14.5” (37 cm) long: catalogue number 9473, lot number 0689812, and date of distribution from 16 november 2012 through 4 january 2013 during an in-process inspection, terumo cvs identified the presence of loose fiber particulate that exceeded finished product specifications on certain product lots of sarns soft-flow aortic cannulae and sarns venous return cannulae. the presence of loose fiber particulate on the surface or inside of the cannulae tubing may be difficult for users to detect. if loose fiber particulate is present, it could be deposited in the patient’s vascular system resulting in varying degrees of patient harm depending on the size of the dislodged material, the location in which it is deposited, and the condition of the patient. potential outcomes include particulate embolism or an inflammatory response which can create clot, ischemia, or tissue death. terumo cvs has not received any reports of loose particulate from customers and there are no reported injuries from the observed defect. the manufacturer advises users to stop using sarns soft-flow cannulae and sarns venous return cannulae from the affected lots and return all unused affected products to them. according to the local supplier, the affected products were not distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 24 october 2013.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Terumo Sarns Soft-Flow Aortic Cannulae and Sarns Venous Return Cannulae
  • Manufacturer

Manufacturer