Viewray, Inc. recalls
Every recall we track for Viewray, Inc. — 6 in all, from 2019–2021 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Viewray, Inc. peaked in 2019 (3); 6 since 2017.
All FDA recall records for Viewray, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 1 | 1 | 1 | 3 |
| 2020 | 0 | 2 | 0 | 0 | 2 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Viewray, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Viewray, Inc. recalls
5 shown- Lower riskMedical device
Viewray, Inc. recalls ViewRay MRIdian Linac System: Model No. 20000-01 software, CE 0086 - Product Usage: intended to be used for planning
ViewRay recalls specific software versions for French, German, and Italian language settings in their MRIdian Linac System due to treatment delivery anomalies. Affected units may require software updates or corrections to ensure safe radiation therapy planning.
ViewRayMay 4, 2021 - Use cautionMedical device
Viewray, Inc. recalls ViewRay MRIdian System: Model No. 10000, CE, Rated Supply Voltage - 380/480 VAC, 3 - Frequency Range (Hertz) - 50/60
ViewRay recalls its MRIdian System Model 10000 due to potential overheating of receive coil components that could cause burns during use. Affected units include all lots/serial numbers sold globally.
ViewRayOct 20, 2020 - Use cautionMedical device
Viewray, Inc. recalls ViewRay System: Model No. 10000 and 20000 for radiation treatment. PN11440 MRIdian System Treatment Planning and
ViewRay System models 10000 and 20000 for radiation treatment may have misalignment in dose registration causing incorrect radiation doses. Affected units include specific serial numbers listed in the recall notice.
ViewRayNov 18, 2019 - UnratedMedical device
Viewray, Inc. recalls MRIdian Linac Radiation Therapy System, Model 20000.
Viewray recalls its MRIdian Linac Radiation Therapy System Model 20000 due to potential dose calculation discrepancies between adaptive optimizations and AQA calculations. Affected units have specific serial numbers listed in the recall.
ViewrayMar 18, 2019 - Lower riskMedical device
Viewray, Inc. recalls MRIdian Linac Radiation Therapy System Model 10000 and 20000
Viewray recalls specific MRIdian Linac models due to inadequate instructions for transferring radiation treatment plans between systems, potentially causing treatment errors. Affected units include Model 10000 and 20000 with listed serial numbers.
ViewrayMar 3, 2019
Viewray, Inc. recall questions
How many recalls has Viewray, Inc. had?
6 recalls from Viewray, Inc. are on record with U.S. safety agencies, from 2019–2021.
What is the most recent Viewray, Inc. recall?
Viewray, Inc. recalls ViewRay MRIdian Linac System: Model No. 20000-01 software, CE 0086 - Product Usage: intended to be used for planning, dated May 4, 2021. Every Viewray, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Viewray, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Viewray, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.