FDA Device recall Z-0806-2016
MRIdian ViewRay Radiation Therapy System, VIEWRAY Inc
- FDA Device
- Class II
- terminated
- Published 2016-02-24
On 2016-02-24 the FDA classified a Class II recall of MRIdian ViewRay Radiation Therapy System, VIEWRAY Inc by Viewray, citing the system loaded a completion fraction in the incorrect order after a treatment interruption.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0806-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-12-24 |
| Published | 2016-02-24 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Viewray |
| Distribution | CA, FL, MO, WI |
Product
MRIdian ViewRay Radiation Therapy System, VIEWRAY Inc.
Reason
The system loaded a completion fraction in the incorrect order after a treatment interruption.
Identifiers
| code_info | Model #: 10000, Serial #'s: 100, 101, 102, 104 & 105 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0806-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.