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 Recalled by Eos Imaging Inc Due to When performing calibration, an alert message on the...

Date: February 17, 2015
Company: Eos Imaging 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 Eos Imaging Inc directly.

Affected Products

EOS, Digital radiography system used in general radiographic examinations.

Quantity: 13 units installed in US

Why Was This Recalled?

When performing calibration, an alert message on the spectral filtration of the X-ray beam may be suppressed. Improper filtration of the X-ray Beam can then occur in exams set up with copper filtration.

Where Was This Sold?

This product was distributed to 9 states: CA, DE, FL, IL, IN, MN, MO, OH, PA

Affected (9 states)Not affected

About Eos Imaging Inc

Eos Imaging Inc has 2 total recalls tracked by RecallDetector.

Related Recalls

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