# FDA recall Z-2587-2023

> **PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.** · Class II · device recall initiated 2023-08-15.

## Product

Philips Allura Xper, Allura Centron, Allura CV, Azurion, UNIQ Clarity, and MultiDiagnost-Eleva systems

## Reason for recall

A damaged foot switch may cause instances where no or only intermittent x-ray radiation initiation is possible.

## Distribution

Worldwide distribution

## Key facts

- **Recall number:** Z-2587-2023
- **Recalling firm:** PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-08-15
- **Report date:** 2023-09-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Best, Netherlands

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2587-2023

## Citation

> AI Analytics. FDA recall Z-2587-2023. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2587-2023. Source: US FDA. Licensed CC0.

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