Class II — Potential Health Hazard

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

Proteus 235 and Proteus ONE proton therapy systems Recalled by Ion Beam Applications S.A. Due to Recall is being initiated to address on-site software...

Date: May 18, 2016
Company: Ion Beam Applications S.A.
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 Ion Beam Applications S.A. directly.

Affected Products

Proteus 235 and Proteus ONE proton therapy systems

Quantity: 18 worldwide and 10, in the U.S.

Why Was This Recalled?

Recall is being initiated to address on-site software installations not being performed consistently with IBA standard operating procedures.

Where Was This Sold?

This product was distributed to 10 states: FL, IL, LA, NJ, OK, PA, TN, TX, VA, WA

Affected (10 states)Not affected

About Ion Beam Applications S.A.

Ion Beam Applications S.A. has 36 total recalls tracked by RecallDetector.

Related Recalls

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