CAS I/II Absorbers installed in the BleaseSirius and BleaseFocus Anesthesia Workstations 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Spacelabs 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
    2013-11-28
  • 사례 출판 날짜
    2013-11-28
  • 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: spacelabs healthcare cas i/ii absorbers installed in the bleasesirius and bleasefocus anesthesia workstations the united states food and drug administration (fda) has issued a medical device safety alert concerning the recall of cas i/ii absorbers installed in the bleasesirius and bleasefocus anesthesia workstations, manufactured by spacelabs healthcare. the affected products are identified as follows: part no.: 12200900, 12200901, 12200902, 12200903, 14200100 service kits part number: 050-0659-00 and 050-0901-00 manufacturing date: 21 feb 2013 through 30 sep 2013 due to a potential defect in the affected products, the bag to-vent switch in cas i/ii absorbers may fail due to loose fastening hardware in an absorber. in the worst case, this would result in a large leak from the absorber circuit while operating in bag mode and could impede the ability to provide ventilation in bag mode. operation in vent mode along with all monitoring and alarm functions will continue to operate normally. customers with questions were advised to contact spacelabs healthcare for technical support. for details, please visit the following fda websites: http://www.Fda.Gov/safety/medwatch/safetyinformation/safetyalertsforhumanmedicalproducts/ucm376772.Htm http://www.Fda.Gov/medicaldevices/safety/listofrecalls/ucm376764.Htm if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 28 november 2013.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 의료기기 분류등급
  • 제품 설명
    Medical Device Safety Alert: Spacelabs Healthcare CAS I/II Absorbers installed in the BleaseSirius and BleaseFocus Anesthesia Workstations
  • Manufacturer

Manufacturer