22mm Flextube Transport Breathing Systems with non-rebreathing valve 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Intersurgical Limited 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
    2017-08-22
  • 사례 출판 날짜
    2017-08-22
  • 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: intersurgical 22mm flextube transport breathing systems with non-rebreathing valve the medicines and healthcare products regulatory agency (mhra) of the united kingdom posted a field safety notice concerning 22mm flextube transport breathing systems with non-rebreathing valve, manufactured by intersurgical limited. [ref numbers: 2070000, 2070001, 2073000, 2074000, 2075000 and 5020002; lot numbers: from 31258704 to 31755743] the manufacturer has voluntarily initiated a global recall of specific product codes and associated lots above of the 22mm flextube transport breathing systems with nonrebreathing valve. a fault has been identified in a non-rebreathing valve component in the affected products, and could result in an occlusion due to the valve sticking. if a ventilator with no self test facility is being used the fault may not be identified. the outcome for the patient will depend on a number of variables, including the degree of occlusion and how quickly the source of the problem is identified allowing remedial action to be taken. according to the manufacturer, an internal assessment of product performance has confirmed that these devices can potentially raise serious risk to the patient. for this reason and to address any potential risk of harm, the affected products should not be used and should be destroyed. the affected users are advised to stop the use of all affected devices immediately and ensure they are quarantined and destroyed. the manufacturer is working to resolve this situation and in the meantime they have an alternative replacement for the systems that do not have an adjustable peep valve or monitoring line (alternative product code 2080004). for details, please refer to the following link: https://www.Gov.Uk/drug-device-alerts/field-safety-notice-14-to-18-august-2017 if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 22 august 2017.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Intersurgical 22mm Flextube Transport Breathing Systems with non-rebreathing valve
  • Manufacturer

Manufacturer