BCI Remote Alarm Cables 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Smiths Medical ASD 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
    2013-04-10
  • 사례 출판 날짜
    2013-04-10
  • 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: smiths medical bci remote alarm cables the united states food and drug administration (fda) has posted a medical device safety alert issued by medical device manufacturer, smiths medical asd, concerning its bci remote alarm cables (no=normally open, nc=normally closed), used with 9004 the capnocheck capnography (plus or sleep) system, reorder numbers: ww3398no & ww3398nc [lot no.: ww3398no0820, ww3398no0847, ww3398no0948, ww3398nc0822, ww3398nc0847, and ww3398nc0947]. these cables were distributed in colorado, illinois, indiana, massachusetts, south carolina, and wisconsin from october, 2008 through september, 2012. the bci remote alarm cables are designed for use with the 9004 capnocheck capnography (plus or sleep) system to transfer alarm signals from the capnocheck capnography system to a remote alarm system. the manufacturer has become aware that, in rare instances, the bci remote alarm cables (bci cables) are not transferring alarms when used with some remote nurse alarm systems. these products may cause serious adverse health consequences, including death. according to fda, the manufacturer has notified its customers by an “urgent medical device field safety notice-recall” letter to instruct customers to inspect their inventory and remove all affected devices from use. for details, please visit the following fda website: http://www.Fda.Gov/medicaldevices/safety/listofrecalls/ucm347193.Htm if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 10 april 2013.

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