Class II — Potential Health Hazard

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

MEVION S250i Recalled by Mevion Medical Systems, Inc. Due to Treatment is allowed to continue (via partials) in...

Date: October 1, 2018
Company: Mevion Medical Systems, 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 Mevion Medical Systems, Inc. directly.

Affected Products

MEVION S250i

Quantity: 1 unit

Why Was This Recalled?

Treatment is allowed to continue (via partials) in situations where dDose1 interlock has tripped

Where Was This Sold?

This product was distributed to 1 state: DC

Affected (1 state)Not affected

About Mevion Medical Systems, Inc.

Mevion Medical Systems, Inc. has 14 total recalls tracked by RecallDetector.

Related Recalls

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