---
title: "IBA Proton Therapy System - PROTEUS 235- Designed to produce and deliver a pr... — FDA record Z-2693-2024 | Is It on Recall"
description: "Temporary deactivation of collision detection for Forte Robotic Patient Positioning System occasionally experiences issues"
url: https://isitonrecall.com/recall/fda-device-z-2693-2024-iba-proton-therapy-system-proteus-235-designed-to-produce-and-deliver-a-proton-beam-for-the-treatmen/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# IBA Proton Therapy System - PROTEUS 235- Designed to produce and deliver a proton beam for the treatment of patients ... — FDA record Z-2693-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jul 10, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: IBA Proton Therapy System - PROTEUS 235- Designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation
- **Reason**: Temporary deactivation of collision detection for Forte Robotic Patient Positioning System occasionally experiences issues
- **Classification**: Class II
- **Recalling firm**: Ion Beam Applications S.A.
- **Quantity**: 19 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2693-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2693-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI-DI: (01)05404013801138 Serial Numbers; PAT.108 (US), PAT.110 (US), PAT.111 (FR), PAT.112 (US), PAT.113 (US), PAT.114 (CZ), PAT.115 (IT), SAT.116 (US), SAT.117 (PL), SAT.118 (RU), SAT.119 (US), SAT.120 (DE), SAT.122 (SE), SAT.123 (US), SAT.126 (US), SBF.101 (FR), SBF.103 (JP), SBF.104 (JP), SBF.105(US). |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

IL,LA, NJ, MI,OK, TN, TX, VA, WA Foreign: Czech Republic France Germany Italy Japan Poland Russia Sweden

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Illinois](https://isitonrecall.com/state/illinois/)
- [Louisiana](https://isitonrecall.com/state/louisiana/)
- [Michigan](https://isitonrecall.com/state/michigan/)
- [New Jersey](https://isitonrecall.com/state/new-jersey/)
- [Oklahoma](https://isitonrecall.com/state/oklahoma/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)
- [Texas](https://isitonrecall.com/state/texas/)
- [Virginia](https://isitonrecall.com/state/virginia/)
- [Washington](https://isitonrecall.com/state/washington/)

## Dates in the source

- **Report date**: Aug 28, 2024
- **Recall initiation date**: Jul 10, 2024
- **Center classification date**: Aug 21, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2693-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Ion Beam Applications S.A. records](https://isitonrecall.com/brand/ion-beam-applications-s-a/)