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Elekta, Inc. recalls Monaco RTP System Radiation treatment planning
Recalled October 2, 2013 · FDA recall Z-2276-2013 · Elekta
Hazard
Upgrade installation script is designed to overwrite the same pouch files in the Treatment Couch Library with the original default values. · FDA Class II
Units
45
Sold at
Nationwide Distribution including AK, CA, CO, CT, FL, IL, IN, MI, MN, MO, NC, NJ, NY, OH, OK, OR, PA, SC, TN, TX, WA and Puerto Rico.
Description
Upgrade installation script is designed to overwrite the same pouch files in the Treatment Couch Library with the original default values.
Product
Monaco RTP System Radiation treatment planning
Manufacturer(s)
Elekta, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →