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 | IBA identified incorrect screw holes depth in graphite block 8 with respect to the degrader |
| Product | Proteus 235, graphite block 8 |
| Quantity | 3 |
| Distribution | WA |
| Initiated | 2017-10-17 |
| Classified | 2018-03-08 |
| Terminated | 2019-03-29 |
| Recall number | Z-0930-2018 |
| 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-0930-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/79227/
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