ClearanceBrief
Recall Z-0482-2021 ยท IYE Accelerator, Linear, Medical

Viewray, Inc.

ViewRay MRIdian Linac System: Model No. 20000, CE, Rated Supply Voltage - 380/480 VAC, 3 - Frequency Range (Hertz) - 50/60 Hz, Rated Input in Amperes - 210 A, UDI. The MRIdian system and the MRIdian Linac system, with magnetic resonance imaging capabilities, is intended to provide stereotactic radiosurgery and precision radiotherapy for lesions, tumors, and conditions anywhere in the body where

DateOct 20, 2020
StatusTerminated
ReasonThere is a potential that components of the receive coil can reach elevated temperatures which has the potential to cause a burn injury to the patient or user.
Root causeDevice Design
ActionOn 10/20/2020, the firm, ViewRay, Inc, emailed an "Urgent Device Correction" notification to all affected consignees. In addition to informing consignees about the correction, the firm asked consignees to take the following actions.: 1. For Customer using TPDS software ver. 5.2.5 or earlier with optional 3 Plane imaging: - Do: Maintain a distance of at least 5 cm (~2) between the receive coil and the inner surface of the bore wall when using 3 Plane cin treatment imaging (Figure 3 & 4). - Do Not: Select 3 Plane cin treatment imaging if a distance of at least 5 cm (~2) cannot be maintained be
Quantity35 units
DistributionWorldwide Distribution: US (nationwide) to states of: CA, NY, FL, IL, MI, MO, OR, WI and OUS countries of: France, Germany, Italy, United Kingdom, Taiwan, Netherlands, Israel, and Denmark.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K170751MRIdian Linac System with 138-leaf Collimator
Viewray, Incorporated, Jun 7, 2017
K181989MRIdian Linac System
Viewray, Incorporated, Feb 20, 2019