Drug recall
MRIdian ViewRay Radiation Therapy System, VIEWRAY Inc.
FDA recall event 73086 · Class II · Viewray Incorporated
Key facts
| Event ID | 73086 |
|---|---|
| Recall numbers | Z-0806-2016 |
| Recalling firm | Viewray Incorporated |
| Product type | Devices |
| Products | MRIdian ViewRay Radiation Therapy System, VIEWRAY Inc. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The system loaded a completion fraction in the incorrect order after a treatment interruption. |
| Initiation date | Dec 24, 2015 |
| Report date | Feb 24, 2016 |
| Termination date | Feb 22, 2017 |
| City | Oakwood Village |
| State | OH |
| Country | United States |
| FEI number | 3007546534 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: