---
title: "Philips Allura Xper, Allura Centron, Allura CV, Azurion, UNIQ Clarity, and Mu... — FDA record Z-2587-2023 | Is It on Recall"
description: "A damaged foot switch may cause instances where no or only intermittent x-ray radiation initiation is possible."
url: https://isitonrecall.com/recall/fda-device-z-2587-2023-philips-allura-xper-allura-centron-allura-cv-azurion-uniq-clarity-and-multidiagnost-eleva-systems/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Philips Allura Xper, Allura Centron, Allura CV, Azurion, UNIQ Clarity, and MultiDiagnost-Eleva systems — FDA record Z-2587-2023

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 Aug 15, 2023. 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**: Philips Allura Xper, Allura Centron, Allura CV, Azurion, UNIQ Clarity, and MultiDiagnost-Eleva systems
- **Reason**: A damaged foot switch may cause instances where no or only intermittent x-ray radiation initiation is possible.
- **Classification**: Class II
- **Recalling firm**: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- **Quantity**: 19,115 systems
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2587-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2587-2023%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 | Models: 708032, 708034, 708036, 708037, 708038, 722001, 722002, 722003, 722005, 722006, 722008, 722010, 722011, 722012, 722013, 722015, 722019, 722020, 722022, 722023, 722025, 722026, 722027, 722028, 722029, 722031, 722033, 722035, 722038, 722039, 722058, 722059, 722063, 722064, 722065, 722066, 722067, 722068, 722078, 722079, 722221, 722222, 722223, 722224, 722225, 722226, 722227, 722228, 722280, 722400 No UDI-DI information for foot switch component. |

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

## Distribution

Worldwide distribution

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Sep 20, 2023
- **Recall initiation date**: Aug 15, 2023
- **Center classification date**: Sep 14, 2023

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-2587-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. records](https://isitonrecall.com/brand/philips-medical-systems-nederland-b-v/)