Class II — Potential Health Hazard

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

DRX Revolution Mobile X-Ray System Recalled by Carestream Health, Inc. Due to Unexpected failure of electrical components within the CPI...

Date: October 2, 2023
Company: Carestream Health, Inc.
Status: Ongoing
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 Carestream Health, Inc. directly.

Affected Products

DRX Revolution Mobile X-Ray System

Quantity: 3,961 units

Why Was This Recalled?

Unexpected failure of electrical components within the CPI generator.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Carestream Health, Inc.

Carestream Health, Inc. has 17 total recalls tracked by RecallDetector.

Related Recalls

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