Class II — Vision Rt Inc
| Recalling firm | VISION RT LIMITED |
|---|---|
| Registered facility | View this company's 3 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Potential use error when the external Gate Controller is turned ON after the Vision RT software has been opened. |
| Product | AlignRT is a video-based three-dimensional (3D) surface imaging system which is used to image the skin surface of a patient in 3D before and during radiotherapy treatment. |
| Quantity | 55 |
| Distribution | Nationwide Distribution |
| Initiated | 2014-11-11 |
| Classified | 2015-01-07 |
| Terminated | 2016-05-11 |
| Recall number | Z-0934-2015 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Vision Rt Inc (Z-0934-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/70009/
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