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[Recalled] Proteus 235, Proton Therapy System Product Usage: The Proton Therapy System - Proteus 235 is a medical device designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditi
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | Proteus 235, Proton Therapy System Product Usage: The Proton Therapy System - Proteus 235 is a medical device designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation. The PTS may include a fixed |
|---|---|
| Brand / manufacturer | Ion Beam Applications S.A. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2684-2017 |
| Country of notice | Belgium |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 13 December 2016 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Software issue
This Class II recall concerns device products distributed in Belgium and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Ion Beam Applications S.A.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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