Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

VersaCell X3 Solution and VersaCell X3 Expansion Pack Recalled by Siemens Medical Solutions Diagnostics Due to The keyboard and monitor may not be properly...

Date: April 25, 2014
Company: Siemens Medical Solutions Diagnostics
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Siemens Medical Solutions Diagnostics directly.

Affected Products

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.

Quantity: 19 units

Why Was This Recalled?

The keyboard and monitor may not be properly secured to the monitor arm.

Where Was This Sold?

Worldwide Distribution - USA including Iowa and New York and Internationally to Canada, Chile, France, India, Italy, Malaysia, Peru, Korea, and the United Kingdom.

About Siemens Medical Solutions Diagnostics

Siemens Medical Solutions Diagnostics has 8 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report