ROSA Brain and ROSA One Surgical Robots 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Surgicom 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-2017-RN-00699-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2017-05-26
  • 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
    Medtech has identified a potential software issue for certain rosa brain and rosa one devices than can prevent it reaching a planned trajectory. when the robot arm is automatically sent onto a trajectory, cartesian coordinates are converted to joint configuration through a mathematical model, and for a very limited number of positions, the mathematical model is imperfect and may prevent the robot arm from reaching the desired position.For automatic moves, if the robot is sent to an unreachable trajectory, the device will display an error message and shut down. a delay of surgery can occur.For “isocentric micromoves” mode used during brain surgery, a hazardous situation can occur if an automatic micro movement to trajectory is planned and an instrument is inside the patient anatomy. if not detected by the user, this could lead to ineffective treatment, serious injury, or even death of the patient.To date medtech has not recorded any complaints for this issue.
  • 조치
    Surgicom is currently working on a software correction for this issue, which is expected to be available in July 2017. Surgicom will contact users to arrange for installation of the software update. In the interim, users are to discontinue use of the micromovement function in isocentric mode during brain surgery. In addition, if the issue occurs for other automatic moves, when the error message "A difference in the expected and the actual robot position has been detected. The device will shut down" is displayed users are advised to follow the directions regarding restart and continuation of use of the device that are included in the customer letter.

Device

  • 모델명 / 제조번호(시리얼번호)
    ROSA Brain and ROSA One Surgical RobotsROSA Brain 3.0.0 Robotic Surgical AssistantSerial Number: BR15002ROSA One 3.1.0 Robotic Surgical AssistantSerial Number: BS16001ARTG Number: 235379 and 278903
  • Manufacturer

Manufacturer

  • Source
    DHTGA