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Ion Beam Applications S.A. recalls Proteus 235
Recalled April 5, 2017 · FDA recall Z-1695-2017 · Ion Beam Applications S.A
Hazard
The Proton Therapy System can allow gantry rotation even if the snout is not properly locked. · FDA Class II
Units
8 worldwide, 4 in U.S.
Sold at
Distributed in MA, FL, VA, and TN. China, South Korea, France and Germany
Description
The Proton Therapy System can allow gantry rotation even if the snout is not properly locked.
Product
Proteus 235
Manufacturer(s)
Ion Beam Applications S.A.
Made in
Belgium
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →