Generator Gen11 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 ETHICON Endo-Surgery 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
    2018-03-01
  • 사례 출판 날짜
    2018-03-01
  • 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: ethicon generator gen11 medical device manufacturer, ethicon endo-surgery, has issued a medical device safety alert concerning its ethicon generator gen11 (gen11). the manufacturer has confirmed a cybersecurity software vulnerability and is issuing a field cybersecurity routine update and patch to address that vulnerability on the gen11. the cybersecurity software vulnerability can exist when using the gen11 system with certain non-oem disposable devices as is it possible for these devices to bypass the gen11 security authentication. according to the manufacturer, the cybersecurity software vulnerability has been assessed to have a sufficiently low (acceptable) residual risk of patient harm because the gen11 has additional safeguards in place to protect the patient even though it is possible for the gen11 security authentication to be bypassed. the gen11 neither has wireless connection nor connects to any it networks. the generator does not store any patient record and there is no impact on patient privacy. since the vulnerability represents a low risk of harm to patients, health care practitioners who have treated patients using the gen11 may continue to follow those patients post-operatively in the usual manner. after the update of the gen11 to address the cybersecurity software vulnerability, some of the non-oem products may no longer work on it. oem ethicon (including sterilmed) devices will continue to function as designed on the gen11 systems. the users are strongly recommended to comply with the gen11 product labeling and using only oem devices on the gen11. as referenced in the user manual warnings and precaution section, use of non-oem devices may lead to unanticipated results and possible injury to the user or patient. according to the local supplier, the affected products are distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 1 march 2018.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: ETHICON Generator Gen11
  • Manufacturer

Manufacturer