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Elekta, Inc. recalls Monaco Product Usage: Planning of radiation therapy
Recalled July 18, 2012 · FDA recall Z-2007-2012 · Elekta
Hazard
Incorrect patient shift directions when the Setup reference dialog is printed out when the DICOM coordinates option is enabled for reports. · FDA Class II
Units
38
Sold at
US Nationwide Distribution - including the states of: CA, CT, FL, IL, IN, KY, MI, MN, MO, NJ, NY, NC, OH, OK, OR, PA, WA, and WI
Description
Incorrect patient shift directions when the Setup reference dialog is printed out when the DICOM coordinates option is enabled for reports.
Product
Monaco Product Usage: Planning of radiation therapy
Manufacturer(s)
Elekta, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →