Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Siemens AXIOM Artis zeego x-ray Recalled by Siemens Medical Solutions USA, Inc Due to Siemens issued a customer safety notice about the...

Date: May 13, 2013
Company: Siemens Medical Solutions USA, Inc
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 USA, Inc directly.

Affected Products

Siemens AXIOM Artis zeego x-ray, angiographic system

Quantity: 132

Why Was This Recalled?

Siemens issued a customer safety notice about the overlay of system information after a functional check of the brakes on the Artis Zeego system.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Siemens Medical Solutions USA, Inc

Siemens Medical Solutions USA, Inc has 613 total recalls tracked by RecallDetector.

Related Recalls

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