Recall
RoboCouch Patient Support System, model number 025007, a subsystem of the Cyberknife Robotic Radiosurgery System, manufactured by Accuray Incorporated, Sunnyvale, CA. Intended for use in the support and positioning of a patient during…
Accuray Inc · 21 July 2009
- Status
- Recall terminated
- Why, in the FDA's words
- “Mechanical Failure-- Patient Support System's table top may unexpectedly descend several inches.”
- Recall began
- 21 July 2009
- Company
- Accuray Inc
- Device type
- Product code (JAI)
- 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.