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
Accelerator, linear, medical - Product Code IYE
원인
Potential use error when the external gate controller is turned on after the vision rt software has been opened.
조치
VisionRT sent an Urgent Medical Device Correction Notification letter dated November 10, 2014, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers shall:
A. Print the instructions in Appendix 3, place them in the front of the product guide and ensure these instructions are read and understood by all those who need to be aware of them within their organisation;
B. Maintain awareness of this issue until all actions indicated in this letter have been successfully completed;
C. Promptly inform Vision RT if they believe that patient harm occurred due to this issue; AND
D. Complete the acknowledgement in Appendix 1 and return it via email to corrections@visionrt.com.
Contact Vision RT
Should you have any queries on this letter, please do not hesitate to contact Vision RT by telephone on +44 20 83464300 (866 778-2379 from the US) or as per http://www.visionrt.com/contact/details.
For questions regarding this recall call 866-594-5443.
AlignRT is a video-based three-dimensional (3D) surface imaging system which is used to image the skin surface of a patient in 3D before and during radiotherapy treatment.