Home / Recalls / Medical Devices
Elekta, Inc. recalls Monaco RTP System. Radiation treatment planning.
Recalled February 27, 2013 · FDA recall Z-0841-2013 · Elekta
Hazard
The beam is displayed at the "gantry" angle, but the dose is calculated at the "rotation_start" angle. · FDA Class II
Units
13
Sold at
Nationwide Distribution-including the states of AK, CA, FL, NJ, NC, OH, OR, TN, TX, WA, and WI.
Description
The beam is displayed at the "gantry" angle, but the dose is calculated at the "rotation_start" angle.
Product
Monaco RTP System. Radiation treatment planning.
Manufacturer(s)
Elekta, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →