# FDA device recall: Philips Allura Xper with the following Model Numbers: Model # 722001 for Allura Xper FD10C; Model # 722002 for Allura Xp

> recall · VERIFIED · 2026-05-18

Firm: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. · Class II · Philips Allura Xper and MultiDiagnost-Eleva systems  Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended  radiation exposure and additional contra

- Company: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Sector: medtech
- Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Source: MedFuel Intel news monitor. Verification tier: VERIFIED. Informational only, not investment advice. Corrections: media@medfuelinc.com.