FDA Device recall Z-0930-2018
Proteus 235, graphite block 8
- FDA Device
- Class II
- terminated
- Published 2018-03-14
On 2018-03-14 the FDA classified a Class II recall of Proteus 235, graphite block 8 by Ion Beam Applications, citing IBA identified incorrect screw holes depth in graphite block 8 with respect to the degrader.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0930-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-10-17 |
| Published | 2018-03-14 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ion Beam Applications |
| Distribution | WA |
Product
Proteus 235, graphite block 8
Reason
IBA identified incorrect screw holes depth in graphite block 8 with respect to the degrader
Identifiers
| code_info | PAT.115, SAT.116 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
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All Ion Beam Applications recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0930-2018%22
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