Patient Side Manipulators - da Vinci S, Si, Si-e Surgical System (robotic surgical unit)Manufactured from October 2012 to April 2013 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-2013-RN-01248-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2013-11-27
  • 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
    Intuitive surgical has become aware that friction within certain patient side manipulators (ie, instrument arms) can interrupt smooth instrument motion. this interruption is felt by the surgeon as resistance in the movement of the mast. in this situation, the instrument can stall momentarily and then suddenly catch up to the master position if the surgeon pushes through the resistance. this resistance is most noticeable when moving the instrument at very slow speeds and during small movements of the masters. this system behaviours is not autonomous instrument motion. the variable function is immediately apparent to the surgeon, and they would exercise surgical judgment to continue use in only situations where the risk is low. however, they would not necessarily be anticipating an interruption of smooth instrument motion, so may not avoid all vulnerable structures.
  • 조치
    Device Technologies is testing affected Patient Side Manipulators (instrument arms) and replacing or repairing instrument arms as required. Device Technologies in providing work around instructions for users to follow as an interim measure.

Device

  • 모델명 / 제조번호(시리얼번호)
    Patient Side Manipulators - da Vinci S, Si, Si-e Surgical System (robotic surgical unit)Manufactured from October 2012 to April 2013ARTG Number: 97348
  • Manufacturer

Manufacturer