Recall
Accuracy Cyberknife Robotic Radiosurgery System, medical charged particle radiation therapy device. Model number 020700 (axum/standard treatment couch) and 021756 hand controller. The device is indicated for treatment planning and…
Accuray Inc · 1 May 2008
- Status
- Recall terminated
- Why, in the FDA's words
- “Couch may move unexpectedly, which may result in patient impacting the linear accelerator.”
- Recall began
- 1 May 2008
- Company
- Accuray Inc
- Device type
- Product code (IYE)
- Concerns
- K072504
What it means
A recall is the FDA's record that a company is correcting or removing a device because of a problem. Many are fixed with a software update or new instructions; the record does not say whether anyone was hurt. See our plain guide to FDA terms.
The record
The FDA publishes this record in its public device database. The summary documents the company filed, when available, are linked from the FDA's page.