cardiovit at-102 plus 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Schiller Medical 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
    2017-02-08
  • 사례 출판 날짜
    2017-02-08
  • 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: schiller medical cardiovit at-102 plus medical device manufacturer, schiller medical, has issued a medical device safety alert concerning its cardiovit at-102 plus (software version: 1.21; 1.22 or 1.23 and article number: 0.075000) it has recently come to the manufacturer’s attention that patient data mix-up may happen when the setting of “manual send” and “automatic erase after send” is chosen for the data transmission. according to the manufacturer, electrocardiography (ecg) data interchange only happens with this particular setting. all other settings are not affected. the occurrence is evaluated as rare, considering the limited number of incident reports in relation to the number of ecgs made per year and due to the fact that most customers use auto transmission, and additionally to the fact that data interchange is not likely to happen if the patient is released from the cables before the manual ecg transmission is started. the affected users are advised to check their stock and devices on the field to identify the software version of cardiovit at-102 plus. if the software version is either 1.21, 1.22 or 1.23, they need to take actions as recommended below. until receiving a new software version of cardiovit at-102 plus from the manufacturer, affected users are advises to take one of the following three settings to prevent the occurrence of the patient safety issue: automatic send with automatic erase of data after sending automatic send without automatic erase of data after sending manual send without automatic erase of data after sending the manufacturer will deliver a new software version to address this issue and will be released by february 2017. according to the manufacturer, the affected products are not distributed in hong kong. if you are in possession of the products, please contact your supplier for necessary actions. posted on 8 february 2017.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: CARDIOVIT AT-102 Plus
  • Manufacturer

Manufacturer