PlainRecalls
FDA Devices Moderate Class II Terminated

Monaco Radiation Treatment Planning (RTP) System

Reported: March 6, 2019 Initiated: February 8, 2019 #Z-0965-2019

Product Description

Monaco Radiation Treatment Planning (RTP) System

Reason for Recall

If Improve Target Dose was chosen as an optimization model in a previous treatment session, Monaco¿ will automatically use this optimization model again when proceeding with the online plan adaptation of a completion plan when it should not.

Details

Recalling Firm
Elekta, Inc.
Units Affected
14 devices
Distribution
Domestic distribution to Wisconsin, Texas. International distribution to Denmark, England, Germany, Netherlands, Sweden.
Location
Atlanta, GA

Frequently Asked Questions

What product was recalled?
Monaco Radiation Treatment Planning (RTP) System. Recalled by Elekta, Inc.. Units affected: 14 devices.
Why was this product recalled?
If Improve Target Dose was chosen as an optimization model in a previous treatment session, Monaco¿ will automatically use this optimization model again when proceeding with the online plan adaptation of a completion plan when it should not.
Which agency issued this recall?
This recall was issued by the FDA Devices on March 6, 2019. Severity: Moderate. Recall number: Z-0965-2019.