pacemakers REPLY (D, DR, VDR and SR models), ESPRIT (D, DR, S and SR models) and FACIL (DR model) 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Sorin CRM S.R.L 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
    2013-11-20
  • 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
    Press release
  • 원인
    Safety alert on three sorin pacemakers the department of health (dh) today (november 20) drew public attention to a safety notice issued by a local medical device supplier, innotronik hong kong limited, on the overestimation of the residual longevity displayed by the programmer for three models of pacemakers manufactured by sorin crm s.R.L. the affected devices are reply (d, dr, vdr and sr models), esprit (d, dr, s and sr models) and facil (dr model). the manufacturer received several reports in which the devices' elective replacement indicator indicating the time for elective replacement had been reached while the time to elective replacement indicated by the programmer during previous follow-up was at a later date. "when the device approaches the time for elective replacement, such an overestimation of the residual longevity could lead to time for elective replacement or even end of life (eol) being reached between two follow-up consultations. yet, as the first implantation of the pacemakers concerned in hong kong was in 2010 and the overall longevity is not affected, the affected devices are still well ahead of the time for elective replacement and eol," a spokesman for the dh explained. sorin said that no permanent injuries or deaths have occurred in connection with the issue. a new programmer version will be released to correct the problem. according to innotronik, some 400 patients from both public and private hospitals were implanted with the affected devices in hong kong and the company has informed the hospital authority and the relevant physicians of the affected private hospitals. "the dh has not received reports of any local adverse incidents in connection with the use of the affected devices so far," the spokesman remarked. "patients with the affected devices who are feeling unwell or in doubt should promptly consult their health-care professionals," the spokesman advised. the dh has informed relevant stakeholders about the alert and shall continue to liaise with innotronik on the follow-up actions. ends.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Press release: Safety alert on three Sorin pacemakers
  • Manufacturer

Manufacturer