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Elekta, Inc. recalls Monaco - Radiation Treatment Planning used to make treatment plans for patients with prescriptions for external beam ra
Recalled November 4, 2015 · FDA recall Z-0181-2016 · Elekta
Hazard
Unintended update of Dose and MU and Incorrect Assignment of Bolus. · FDA Class II
Units
154
Sold at
CA, IN, MI,MO, TX, WI, Australia, Canada, Germany,m Greece, India, Netherlands, New Zealand, Turkey and United Kingdom
Description
Unintended update of Dose and MU and Incorrect Assignment of Bolus.
Product
Monaco - Radiation Treatment Planning used to make treatment plans for patients with prescriptions for external beam radiation therapy.
Manufacturer(s)
Elekta, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →