Viewray Incorporated: Medical Device Recall in 2016 - (Recall #: Z-0806-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

MRIdian ViewRay Radiation Therapy System, VIEWRAY Inc.

Product Classification:

Class II

Date Initiated: December 24, 2015

Date Posted: February 24, 2016

Recall Number: Z-0806-2016

Event ID: 73086

Reason for Recall:

The system loaded a completion fraction in the incorrect order after a treatment interruption.

Status: Terminated

Product Quantity: 5 units

Code Information:

Model #: 10000, Serial #'s: 100, 101, 102, 104 & 105

Distribution Pattern:

US Distribution to the states of : CA, FL, MO & WI., and Internationally to Republic of Korea.

Voluntary or Mandated:

Voluntary: Firm initiated