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Ion Beam Applications S.A. recalls Proteus 235, Proton Therapy System a medical device designed to produce and delivers a proton beam for the treatment of
Recalled March 21, 2018 · FDA recall Z-0938-2018 · Ion Beam Applications S.A
Hazard
There is a risk of misalignment of the patient when using treatment plans with multiple isocenters. · FDA Class II
Units
37
Sold at
Nationally
Description
There is a risk of misalignment of the patient when using treatment plans with multiple isocenters.
Product
Proteus 235, Proton Therapy System a medical device designed to produce and delivers a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation.
Manufacturer(s)
Ion Beam Applications S.A.
Made in
Belgium
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →