Recall
RoboCouch Patient Support System, a component of the CyberKnife Robotic Radiosurgery System. Model number 025007, manufactured by Accuray Inc., Sunnyvale, CA The CyberKnife is indicated for treatment planning and imageguided…
Accuray Inc · 30 Oct 2008
- Status
- Recall terminated
- Why, in the FDA's words
- “Product may not be tensioned properly, potentially causing unexpected rotation or descent.”
- Recall began
- 30 Oct 2008
- Company
- Accuray Inc
- Device type
- Product code (JAI)
- Concerns
- K042146
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.