Class II — Potential Health Hazard

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

DR 800. Digital Radiography X-ray System. Recalled by Agfa N.V. Due to Potential for the front lever chain of the...

Date: July 29, 2024
Company: Agfa N.V.
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 Agfa N.V. directly.

Affected Products

DR 800. Digital Radiography X-ray System.

Quantity: 141 units

Why Was This Recalled?

Potential for the front lever chain of the DR 800 table to fail.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Agfa N.V.

Agfa N.V. has 7 total recalls tracked by RecallDetector.

Related Recalls

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