Tec 6 and Tec 6 Plus Vaporizers 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 GE 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
    2013-08-13
  • 사례 출판 날짜
    2013-08-13
  • 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: ge healthcare tec 6 and tec 6 plus vaporizers medical device manufacturer, ge healthcare issued a medical device safety alert concerning all tec 6 and tec 6 plus vaporizers. according to the ge healthcare, the user manual pre-operative check, low pressure leak test at 1% dial setting may not detect the full range of leaks from seal wear degradation in the vaporizers. moreover, the integrity of the vaporizer seal may be affected with tec 6 or tec 6 plus vaporizer remanufactured/ manufactured between 12 aug 2005 and 3 dec 2012, due to wear degradation. for any tec 6 or tec 6 plus vaporizer remanufactured / manufactured between 12 aug 2005 and 3 dec 2012 (aetj29001 to aesr49001), a ge healthcare service representative will schedule a repair to update the vaporizer seal. the leak test failures will get first priority for scheduling repair/replacement the manufacturer advises that the addendum with the field safety notice distributed to the affected users had the 12% low pressure leak test which will aid in determining the integrity of the seal. the manufacturer also provides the following recommendations to the affected users: update the tec 6 and tec 6 plus vaporizers user manual with the addendum given. perform the user manual recommended pre-operative check which includes the low pressure leak test on every vaporizer with the dial turned to the 12% setting instead of the specified 1% setting. discontinue use of the tec 6 or tec 6 plus vaporizer if it does not pass the new low pressure leak at 12%, remove it from service and contact a ge healthcare representative for a repair/replacement. if the vaporizer passes the new low pressure leak test at the 12 % setting, it can be used, however, as detailed in the user manual, users should continue to routinely perform the pre-operative check which includes the low pressure leak test. use a monitor to measure the oxygen and anesthetic agent levels as well as monitoring the bellows position during the use of any anesthesia system. according to the local supplier, the affected products have been distributed to hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 13 august 2013.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: GE Healthcare Tec 6 and Tec 6 Plus Vaporizers
  • Manufacturer

Manufacturer