Mindray V-Series Patient Monitors with 12-lead ECG interpretation capabilities 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Ulco Engineering Pty Ltd 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

의료기기에 문제가 생겼을 경우 제조사가 이를 바로잡거나 시장에서 회수하는 조치를 말한다. 회수(Recall)는 의료기기에 결함이 있거나, 건강에 위협이 되거나, 또는 결함도 있고 건강에도 위협이 될 경우에 발생한다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Recall
  • 사례 ID
    RC-2014-RN-01172-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2014-10-30
  • 사례 국가
  • 사례 출처
    DHTGA
  • 사례 출처 URL
  • 비고 / 경고
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, 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 recall data from the U.S. and Australia.
  • 데이터 추가 비고
  • 원인
    Mindray has identified the following issues:- the 12-lead standard and extended measurement report will include false measurements when the p wave or qrs axis cannot be accurately determined by the algorithm. - the median complex and extended measurement report will display the representative beat as 25% larger than actual signal input. - when a patient date of birth is imported into the v-series from an external source, such as mindray’s gateway, e-gateway, panorama central station or panorama workstation, the age will not pass into the 12-lead ecg interpretation algorithm. the algorithm analysis will use the default adult criteria of “50 year adult” in which case the interpretive statements may be incorrect, depending on the actual age of the patient. any output of the 12-lead ecg interpretation data (e.G. printed records, ecg management system, etc.) will include the issues described above. there have been no reports of injuries associated with these issues.
  • 조치
    Mindray is recommending that users discontinue use of the affected units until the software correction is completed. This action has been closed-out on 26/08/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    Mindray V-Series Patient Monitors with 12-lead ECG interpretation capabilitiesV-series Model Numbers: 1409 & 1410Serial Numbers: EGD16006409, EGD13004678 & EGD0B002460ARTG Numbers: 223384
  • Manufacturer

Manufacturer