Class II — Potential Health Hazard

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

Artis zee systems x-ray Recalled by Siemens Medical Solutions USA, Inc Due to The firm became aware of a potential issue...

Date: January 21, 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

Artis zee systems x-ray, angiographic system

Quantity: 17

Why Was This Recalled?

The firm became aware of a potential issue with Artis zee systems bearing model numbers 10094135, 10094137, and 10094141 equipped with a card collimator from a specific lot where a dislocation of the scatter radiation filter inside the card collimator may occur.

Where Was This Sold?

This product was distributed to 14 states: AZ, AR, CA, CT, FL, IA, KS, KY, MO, MT, NY, OK, PA, WV

Affected (14 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