Class II — Ion Beam Applications S.A.
| Recalling firm | ION BEAM APPLICATIONS S.A. |
|---|---|
| Registered facility | ION BEAM APPLICATIONS S.A. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | 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 |
| Quantity | 2 worldwide, 1 in U.S. |
| Distribution | Distribution in US (to Louisiana), and France. |
| Initiated | 2017-03-21 |
| Classified | 2017-04-17 |
| Terminated | 2018-09-19 |
| Recall number | Z-1830-2017 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Ion Beam Applications S.A. (Z-1830-2017).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/76804/
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