Class II — Potential Health Hazard

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

EOS System X- ray beam Digital radiography system used in Recalled by EOS Imaging Due to EOS imaging discovered during production internal testing that...

Date: November 7, 2013
Company: EOS Imaging
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 EOS Imaging directly.

Affected Products

EOS System X- ray beam Digital radiography system used in general radiographic examinations.

Quantity: 22 EOS systems are installed in US

Why Was This Recalled?

EOS imaging discovered during production internal testing that the X-ray beam collimation set up by the operator at the user interface of the acquisition workstation is different from the actual collimation of the X-ray beam operated by the EOS system during the X-ray acquisition.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About EOS Imaging

EOS Imaging has 5 total recalls tracked by RecallDetector.

Related Recalls

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