Intuitive Surgical Endoscope Instrument Control System - da Vinci Xi Surgical System with P5 software 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Device Technologies 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-01414-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2016-10-31
  • 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
    It has been identified that during an internal test, the left hand control (master) on the surgeon console moved unexpectedly upon the first entry into following mode. the system is in following mode when the surgeon is controlling the instruments at the surgeon console. this behaviour was determined to be associated with a software anomaly in the da vinci xi surgical system p5 software that can result in unexpected master movement and potential instrument tip movement under certain circumstances. certain interactions with the patient cart (during patient cart docking, or during multi-port procedures, repositioning the instrument arm) can trigger this behaviour upon entering following mode. the surgeon may receive a recoverable error, experience movement of the master controller and/or movement of the associated cannula/instrument in any direction including potential lateral movement. there is a remote probability of patient harm associated with this issue.
  • 조치
    A software update will be released by Intuitive Surgical to address the anomaly which is expected in quarter 1 2017. In the interim, to prevent this event from occurring, users are advised to follow the instructions below during every da Vinci Xi procedure: 1.During Single-Site surgery, after installing each instrument on the sterile adapter, ensure instrument clutch is not activated and press the port clutch* button for that arm. This is only necessary at the beginning of the procedure, directly after the docking. 2.During Multi-Port surgery: - Immediately after docking to a cannula, press the corresponding port clutch button for that arm, and - If adjusting patient clearance and mid-procedure, ensure instrument clutch is not activated and press the corresponding port clutch button for that arm after the adjustment. This action has been closed-out on 11/05/2017.

Device

  • 모델명 / 제조번호(시리얼번호)
    Intuitive Surgical Endoscope Instrument Control System - da Vinci Xi Surgical System with P5 software Model Number: INS-IS4000ARTG Number: 97348
  • Manufacturer

Manufacturer