Device Recall MRIdian ViewRay Radiation Therapy System, ViewRay 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Viewray Incorporated 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
    72166
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-0115-2016
  • 사례 시작날짜
    2015-08-27
  • 사례 출판 날짜
    2015-10-09
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2017-06-09
  • 사례 출처
    USFDA
  • 사례 출처 URL
  • 비고 / 경고
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • 데이터 추가 비고
    System, radiation therapy, radionuclide - Product Code IYE
  • 원인
    Viewray discovered that in the event that an encoder breaks or fails on the patient handling system (phs, or couch), when attempting to restart the system, the couch could move unexpectedly.
  • 조치
    ViewRay sent an Customer Advisory Notice dated August 27, 2015, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer. It is recommended that if you have a patient on the couch and you receive the fault ''The patient table has experienced an unintended movement. This may be due to the patient or operator leaning on the table. Clear the fault and retry. If the problem persists call Service" on the TPDS,first attempt to clear the fault. If it does not clear and requires you to restart the couch software (same switch as restarting the RTCS) you should manually remove the patient from the couch before restarting the system. A software patch to address this issue is planned for early 2016. In the meantime please practice our recommendation of removing the patient from the couch prior to restarting the RTCS. If you have any questions or concerns regarding this issue, please do not hesitate to contact ViewRay Customer Support at support@viewray.com or call the ViewRay¿¿ Customer Support center at 855-286-8875.

Device

  • 모델명 / 제조번호(시리얼번호)
    Catalog/Part Number: 10000; Serial Numbers: 100, 101, 102, & 105
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    US Distribution to the states of : CA, MO and WI., and Internationally to Korea.
  • 제품 설명
    MRIdian¿ ViewRay¿ Radiation Therapy System, ViewRay¿ || Is indicated for stereotactic radiosurgery and precision radiotherapy for lesions, tumors, and conditions anywhere in the body when radiation treatment is indicated.
  • Manufacturer

Manufacturer

  • 제조사 주소
    Viewray Incorporated, 2 Thermo Fisher Way, Oakwood Village OH 44146-6536
  • 제조사 모회사 (2017)
  • Source
    USFDA