Events

Hamilton/47244/Ventilators 의 리콜

New Zealand Medicines and Medical Devices Safety Authority에 따르면, 해당 리콜 는 New Zealand 에서 Hamilton Medical AG 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
    19875
  • 사례 시작날짜
    2016-03-18
  • 사례 국가
    New Zealand
  • 사례 출처
    NZMMDSA
  • 사례 출처 URL
    https://medsafe.govt.nz/hot/Recalls/RecallSearch.asp
  • 비고 / 경고
    Data from New Zealand is current through July 2018. All of the data comes from the New Zealand Medicines and Medical Devices Safety Authority, 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 New Zealand.
  • 데이터 추가 비고
    Recalling Organisation: InterMed Medical Ltd, 71 Apollo Drive, Albany, AUCKLAND 1311
  • 원인
    The analysis of the customer complaint has identied an issue related to suctioning with the use of the hamilton-g5 and hamilton-s1 ventilators. after preforming the suctioning manuoeuvre, including disconnecting the patient suctioning and then reconnecting the patient the preset pattern of the ventilation may not continue as expected. this software flaw may lead to either hyperventilation or hypoventilation.
  • 조치
    Software to be upgraded

Device

Hamilton/47244/Ventilators
  • 모델명 / 제조번호(시리얼번호)
    Model: , Affected:
  • Manufacturer
    Hamilton Medical AG

Manufacturer

Hamilton Medical AG