Physio-Control, LIFEPAK 20e Defibrillator/Monitor 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Physio-Control 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
    2018-01-09
  • 사례 출판 날짜
    2017-01-09
  • 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: physio-control, lifepak 20e defibrillator/monitor medical device manufacturer, physio-control, has issued a medical device safety alert concerning its lifepak 20e defibrillator/monitor [model/catalog numbers: 70507-xxxxxx, 99507-xxxxxx; lot number multiple]. the manufacturer is aware that some devices have had power-related failures as customers prepared their device for initial deployment or during use within the first year of distribution. the symptoms of these failures may include unexpected power on and power off, device lock-up, or a failure to power on or off. according to the manufacturer, the failures are the result of the manufacturing process residue located beneath a component mounted on the power printed circuit board assembly (pcba). this has the potential to result in a failure to deliver therapy to the patient and serious injury or death. the manufacturer has not received any adverse events reported as a result of this issue. the manufacturer will contact potential affected users to arrange for a device correction included the replacement of the power pcba. the customers are requested to follow the recommended daily operator’s checklist steps in accordance with lifepak 20e defibrillator/monitor operating instructions – section 7 – maintaining the equipment. if the users experience any of the symptoms described above, contact the manufacturer immediately to arrange servicing to your device. 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 09 january 2017.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Physio-Control, LIFEPAK 20e Defibrillator/Monitor
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DH