Proteus 235 — Class II medical device recall Z-0930-2018
Terminated recall by Ion Beam Applications S.A., reported 2018-03-14, distributed in WA. IBA identified incorrect screw holes depth in graphite block 8 with respect to the degrader
| Recall number | Z-0930-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ion Beam Applications S.A., Louvain La Neuve, N/A, Belgium |
| Recall initiated | 2017-10-17 |
| Classified | 2018-03-08 |
| Reported by FDA | 2018-03-14 |
| Terminated | 2019-03-29 |
| Distributed | WA |
| Quantity | 3 |
Product
Proteus 235, graphite block 8
Reason for recall
IBA identified incorrect screw holes depth in graphite block 8 with respect to the degrader
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0930-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.