PlainRecalls
FDA Devices Moderate Class II Terminated

Monaco RTP System. Radiation treatment planning.

Reported: February 27, 2013 Initiated: February 11, 2013 #Z-0841-2013

Product Description

Monaco RTP System. Radiation treatment planning.

Reason for Recall

The beam is displayed at the "gantry" angle, but the dose is calculated at the "rotation_start" angle.

Details

Recalling Firm
Elekta, Inc.
Units Affected
13
Distribution
Nationwide Distribution-including the states of AK, CA, FL, NJ, NC, OH, OR, TN, TX, WA, and WI.
Location
Atlanta, GA

Frequently Asked Questions

What product was recalled?
Monaco RTP System. Radiation treatment planning.. Recalled by Elekta, Inc.. Units affected: 13.
Why was this product recalled?
The beam is displayed at the "gantry" angle, but the dose is calculated at the "rotation_start" angle.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 27, 2013. Severity: Moderate. Recall number: Z-0841-2013.