Integra Ojemann Cortical Stimulator (Electrical antiseizure brain stimulator) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Integra Neurosciences 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-2013-RN-00467-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2013-05-17
  • 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
    The manufacturer found that if the headphone jack is in use during a surgical procedure with the ocs2 and a non-intended voltage (such as static electricity) comes in contact with the outer case of the unit, that voltage could be transmitted to the patient and could be a potential source of injury.
  • 조치
    Integra is advising users that the device may still be used providing the audio jack is not used. An Integra representative will contact affected customers to arrange for the disabling of the audio jacks and prevent the problem occurring. No reports of this issue have been received from the field.

Device

  • 모델명 / 제조번호(시리얼번호)
    Integra Ojemann Cortical Stimulator (Electrical antiseizure brain stimulator)Catalogue number: OCS2All serial numbers affectedARTG number: 150717
  • Manufacturer

Manufacturer