Class II — Potential Health Hazard

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

Monaco RTP System. Used to make treatment plans for patients Recalled by Elekta, Inc. Due to Incorrect dose after editing beam number an wedge...

Date: January 10, 2017
Company: Elekta, 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 Elekta, Inc. directly.

Affected Products

Monaco RTP System. Used to make treatment plans for patients with prescriptions for external beam radiation therapy.

Quantity: 1999

Why Was This Recalled?

Incorrect dose after editing beam number an wedge angle.

Where Was This Sold?

This product was distributed to 26 states: AZ, AR, CA, CO, GA, IL, IN, LA, MA, MI, MN, MO, NV, NH, NJ, NY, NC, OH, OR, PA, SD, TX, UT, VA, WA, WI

Affected (26 states)Not affected

About Elekta, Inc.

Elekta, Inc. has 100 total recalls tracked by RecallDetector.

Related Recalls

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