FDA Recall Terminated

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.

Recall: Z-0934-2015 · Initiated November 11, 2014

Recall

Recall Number
Z-0934-2015
Event Number
70009
Firm
Vision Rt Inc
FEI Number
3017888782
Product Code
IYE
Status
Terminated
Root Cause
Under Investigation by firm
Initiated
November 11, 2014
Posted
January 7, 2015
Terminated
May 11, 2016
Address
8840 Stanford Blvd, Columbia, MD, 21045-5827

Description

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.

Reason

Potential use error when the external Gate Controller is turned ON after the Vision RT software has been opened.

Action

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 [email protected]. 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.

Distribution

Nationwide Distribution

Quantity

55