Dräger Oxylog Transport Ventilators - Oxylog 3000 and Oxylog 3000plus 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Draeger Medical Australia 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-2016-RN-01617-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2016-12-14
  • 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
    In dec 2015, dräger informed users of an error condition observed with the oxylog 3000 / oxylog 3000plus (tga ref.: rc-2015-rn-01256-1), where the loss of contact of one of the control knobs generated an error message (previously referred to as "poti unplugged"). in these cases, acoustical and visual alarms are triggered, the breathing system releases pressure & the ventilation function stops operating. investigations indicated that the error condition was caused by an oxide layer in the potentiometer. these oxide layers may accumulate over a longer period of time where various factors collude (i.E. if the knobs are moved rarely or never). as communicated previously, a verified remedy is repeated twisting of the knobs that removes the oxide layer. whilst the remedy of twisting the knob is still considered effective, to reduce the impact of this error condition dräger has developed new software.
  • 조치
    Dräger has developed a new software that reduces the impact of the error condition i.e., software version 1.06 will be introduced for the Oxylog 3000plus and software version 1.23 for Oxylog 3000 respectively. A Dräger engineer will contact affected customers directly to schedule the software upgrade. Whenever a "control knob faulty" condition will occur with a device being equipped with the new software, the device will continue to ventilate with the last valid settings, display for example the values for tidal volume in case of a defective potentiometer for VT and post the corresponding alarm. As reflected in the amended Instructions for Use Manual, users are advised to check the patient’s condition and the ventilation.

Device

  • 모델명 / 제조번호(시리얼번호)
    Dräger Oxylog Transport Ventilators - Oxylog 3000 and Oxylog 3000plusAll Serial NumbersARTG Number: 169507
  • Manufacturer

Manufacturer