Every recall we track for Viewray, Inc. — 6 in all — plus the complaints and injury reports the public filed about them.
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.
ViewRay recalls its MRIdian Linac System (Model 20000) due to potential overheating of receive coil components that could cause burns. Affected units include all lots/serial numbers sold globally. No remedy specified in official notice.
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.
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.
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.
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.
