Recall
VersaCell X3 Solution and VersaCell X3 Expansion Pack, a robotic laboratory sample-management system. It connects up to 3 instruments and provides a user interface that routes samples, reduces manual tasks and consolidates results.
Siemens Medical Solutions Diagnostics · 25 April 2014
- Status
- Recall terminated
- Why, in the FDA's words
- “The keyboard and monitor may not be properly secured to the monitor arm.”
- Recall began
- 25 April 2014
- Company
- Siemens Medical Solutions Diagnostics
- Device type
- Product code (LXG)
- Concerns
- K970227
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.