Proteus : Incorrect Screw Holes May Cause Malfunction

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Recalling firmIon Beam Applications S.A.Chemin du Cyclotron, 3, N/A · Louvain La Neuve, N/A N/A

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Ion Beam Applications S.A. is recalling the Proteus 235 graphite block 8 because the screw holes are incorrectly sized. This could lead to malfunction in normal use, but the recall does not include a remedy.

Why it’s dangerous

The graphite block 8 has incorrect screw hole depth, which may cause the component to malfunction. This issue could affect the proper operation of the Proteus 235 device.

Who’s affected

Users of the Proteus 235 graphite block 8 are affected. The risk is likely for those who have the specific model and are using it in normal applications.

How to tell if you have this one

Check for the Proteus 235 model with graphite block 8. The product is identified by the patent numbers PAT.115 and SAT.116.

Brand
Ion Beam Applications S.A.
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Identify if you have the Proteus 235 graphite block 8 with the specified patent numbers.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

The recall is due to incorrect screw hole depth in the graphite block 8, which may cause malfunction in normal use.

Is there a remedy for this issue?

The recall record does not specify a remedy.

How can I tell if I have the recalled product?

Check for the Proteus 235 graphite block 8 with patent numbers PAT.115 and SAT.116.

Take action

Contact Ion Beam Applications S.A.

We’ve drafted a message you can send Ion Beam Applications S.A. to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0930-2018 — Ion Beam Applications S.A. Ion Beam Applications S.A.

Hello,

I own a Ion Beam Applications S.A. that is covered by recall Z-0930-2018 from Ion Beam Applications S.A..

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-0930-2018 (October 17, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0930-2018 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Ion Beam Applications S.A. recalls Proteus 235, graphite block 8

Recall notice