# FDA recall Z-2503-2025

> **PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.** · Class II · device recall initiated 2025-08-01.

## Product

Philips Allura System configured with a 1 Phase UPS. Allura family (R1.x, R2.x).     Labeled as the following with corresponding model numbers:     1. Allura Xper FD10, Model Number 722003    2. Allura Xper FD10/10, Model Number 722005    3. Allura Xper FD20, Model Number 722006    4. Allura Xper FD20 Biplane, Model Number 722008    5. Allura Xper FD10, Model Number 722010    6. Allura Xper FD10/10, Model Number 722011    7. Allura Xper FD20, Model Number 722012    8. Allura Xper FD20 Biplane, Model Number 722013    9. Allura Xper FD20 OR Table, Model Number 722023    10. Allura Xper FD10, Model Number 722026    11. Allura Xper FD10/10, Model Number 722027    12. Allura Xper FD20, Model Number 722028    13. Allura Xper FD20/10, Model Number 722029    14. Allura Xper FD20 OR Table, Model Number 722035    15. Allura Xper FD20/20, Model Number 722038    16. Allura Xper FD20/15, Model Number 722058    17. Allura Xper FD20/15 OR Table, Model Number 722059.

## Reason for recall

Philips Azurion and Allura systems configured  with a 1 Phase Uninterruptible Power Supply (UPS) have the potential of shutting down and/or not starting up, if power to the system is lost.

## Distribution

Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Austria, Belarus, Belgium, Bolivia, Bosnia and Herzegovina, Brazil, Bulgaria, Canada, Chile, China, Colombia, Cyprus, Czech Republic, Dominican Republic, Ecuador, Egypt, Finland, France, Germany, Greece, Hong Kong, Hungary, India, Iran, Ireland, Israel, Italy, Jamaica, Japan, Jordan, Kazakhstan, Korea, Republic of, Kosovo, Latvia, Lithuania, Macedonia, Maldives, Malta, Mexico, Moldova, Netherlands, New Caledonia, New Zealand, Nicaragua, Norway, Panama, Paraguay, Peru, Philippines, Romania, Russian Federation, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland, Taiwan, Tunisia, United Arab Emirates, United Kingdom, Uruguay, Uzbekistan, Viet Nam.

## Key facts

- **Recall number:** Z-2503-2025
- **Recalling firm:** PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-08-01
- **Report date:** 2025-09-10

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2503-2025

## Citation

> AI Analytics. FDA recall Z-2503-2025. Retrieved 2026-08-18 from https://api.ai-analytics.org/recall/Z-2503-2025. Source: US FDA. Licensed CC0.

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