ProductGuru
AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →

[Recalled] Proteus 235-Proton Therapy System — if the user forgets to select the trigger input manually while beam gating is p… | FDA 2021-05-26

recall fda device belgium

A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.

Recall details

ProductProteus 235-Proton Therapy System
Brand / manufacturerIon Beam Applications S.A.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-2155-2021
Country of noticeBelgium
Risk levelClass II
Hazard typerecall
Notice date26 May 2021

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: if the user forgets to select the trigger input manually while beam gating is prescribed for the patient, the proton irradiation will be delivered without gating. If the beam is not gated as prescribed, the treatment field may be delivered with an error in position

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.

Shop Recalled Proteus 235 Proton
Search on Amazon ›Find on eBay ›
As an Amazon Associate and eBay Partner, we may earn from qualifying purchases.

Explore by topic

Looking up a product? Use ProductGuru — free barcode & product database with 35M+ products. Search by EAN / UPC barcode.
Was this page helpful?