Intuitive Surgical Inc. da Vinci Xi Surgical System Patient Cart Arms 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-2015-RN-00291-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2015-04-17
  • 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
    The system reports a “23008” system software fault that indicates a mismatch between the positions reported by the redundant position sensors on one of the patient cart arm joints. the system may fault during start up tests or during use. the system fault is an arm-specific recoverable fault, which leaves the system in a safe state. a fault message will be displayed and the affected arm led colour will change to yellow. the source of the fault is the premature failure of a position sensor located within the faulting joint. there have been no reported injuries as a result of this issue. in a scenario in which the decision is made to convert a procedure to an alternate surgical method due to the error, the patient may be at higher risk of surgical complications because of the historically higher rate of complications in open surgery.
  • 조치
    A Device Technologies representative will contact affected customers to schedule a remote assessment to determine the health of the systems and further schedule an appointment to replace the affected arm. In the interim, users are advised that if the error persists (i.e. the fault cannot be recovered), the affected arm should be disabled and the user should decide to continue the procedure with 3 arms, abort the procedure, or convert to an alternate surgical technique. This action has been closed-out on 9/08/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    Intuitive Surgical Inc. da Vinci Xi Surgical System Patient Cart ArmsInner ArmModel Numbers: 380662-20, 380662-21Outer ArmModel Numbers: 380663-20, 380663-21 Universal Surgical ManipulatorModel Numbers: 380647-20, 380647-22ARTG Number: 97348
  • Manufacturer

Manufacturer