Oxylog Transport Ventilators 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Draeger Medical GmbH 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
    2015-12-28
  • 사례 출판 날짜
    2015-12-28
  • 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: draeger oxylog transport ventilators medical device manufacturer, draeger medical gmbh, has issued a medical device safety alert concerning oxylog transport ventilators manufactured by draeger medical. the affected model numbers are oxylog 2000plus, oxylog 3000 and oxylog 3000plus. the manufacturer has become aware of situations where the error message “poti unplugged" was generated. in those cases, an audible and visual alarm is generated, the breathing system releases pressure and the ventilation function stops operating. according to the manufacturer, no patient injury has been reported due to the issue. the error message is caused by increased electrical contact resistances of the controllers (adjustment potentiometers) that are caused by an oxide layer on the controllers, which accumulates over a longer period of time if the controllers are moved rarely or never. the manufacturer’s product monitoring has shown that some users rarely use the fio2 controller or do not use it at all. as a preventive measure, the manufacturer highly recommends to move all controllers once when the affected device is switched off; at least 10 times to the left and right stop (minimum and maximum value). this measure suffices to clean the resistance taper of the controllers sufficiently. in particular with the error “device malfunction – poti unplugged”, the aforementioned method can also be used to put the device back into operation. the manufacturer reminds users that the affected devices must only be used after verifying its operational readiness. according to the local supplier, the affected products are distributed in hong kong. for details, please refer to the following link:http://apps.Tga.Gov.Au/prod/sara/arn-detail.Aspx?k=rc-2015-rn-01256-1 if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 28 december 2015.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Draeger Oxylog Transport Ventilators
  • Manufacturer

Manufacturer