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Mevion Medical Systems, Inc. recalls MEVION S250 Product Usage: Proton Radiation Therapy System
Recalled November 23, 2016 · FDA recall Z-0411-2017 · Mevion Medical Systems
Hazard
Software defect:2D projection of contours in Verity. The defect causes structures to appear off from their true position in the DRR and the radiograph with an error that increases with the distance of the structure from isocenter · FDA Class II
Units
6 units
Sold at
US Nationwide Distribution in the states of: FL, MO, NJ, OH, OK
Description
Software defect:2D projection of contours in Verity. The defect causes structures to appear off from their true position in the DRR and the radiograph with an error that increases with the distance of the structure from isocenter
Product
MEVION S250 Product Usage: Proton Radiation Therapy System
Manufacturer(s)
Mevion Medical Systems, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →