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Ion Beam Applications S.A. recalls Proteus 235, Proton Therapy System
Recalled April 26, 2017 · FDA recall Z-1830-2017 · Ion Beam Applications S.A
Hazard
In specific circumstances, the user is able to restart an aborted irradiation without having to select the correct partial irradiation data. · FDA Class II
Units
2 worldwide, 1 in U.S.
Sold at
Distribution in US (to Louisiana), and France.
Description
In specific circumstances, the user is able to restart an aborted irradiation without having to select the correct partial irradiation data.
Product
Proteus 235, Proton Therapy System
Manufacturer(s)
Ion Beam Applications S.A.
Made in
Belgium
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →