breathing system components 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Unomedical-A ConvaTec Company should not be used 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
    2011-10-11
  • 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
    Mhra field safety notice: breathing system components the uk medicines and healthcare products regulatory agency (mhra) issued a field safety notice to alert healthcare providers and customers that some products manufactured by unomedical-a convatec company should not be used. according to the manufacturer, there was a logistical error that has occurred in a small number of their medical devices. these devices have been shipped to customers after their intended shelf life has passed and should not be used. the involved devices are: ‧ high vac 600ml bottle with drain and trocar, connecting tube & nrv, ch18 ‧ high vac 600ml bottle with drain and trocar, connecting tube and nrv, ch14 ‧ tracheostomy mask, paediatric ‧ up-mist nebulizer, with "t piece", mouth piece and 2.1m oxygen tubing, adult ‧ ecoclip-3 three of the lots sold past expiry are sterile products. since it cannot be certain that the devices will continue to remain both safe and efficacious in accordance with their intended use, the manufacturer is recalling all the affected devices. the affected devices can be identified by product lot number in conjunction with the product reference number. the lot number and reference number can be found on the device label which is located on both the primary packaging as well as the shipping carton. the affected products are identified as below: product description sterile product? lot number nhs supply chain catalogue codes 26057018 high vac 600ml bottle with drain and trocar, connecting tube & nrv, ch18 yes 040424 n/a 041116 26057014 high vac 600ml bottle with drain and trocar, connecting tube & nrv, ch14 yes 041110 fwx119 246mm tracheostomy mask, paediatric no 03-36 n/a 952mm up-mist nebulizer, with "t piece" mouth piece and 2.1m oxygen tubing, adult no 05-49 fde394 1110130970 ecoclip-3 (this device has now been discontinued) no 4777/4 n/a for details, please refer to the following mhra website: http://www.Mhra.Gov.Uk/safetyinformation/safetywarningsalertsandrecalls/fieldsafetynotices/ index.Htm if you are in possession of the affected products, please stop using them and contact your supplier for necessary actions.

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