# FDA device recall: Philips Azurion systems not configured with an optional auxiliary pan handle. Includes the below product descriptions an

> recall · VERIFIED · 2026-04-28

Firm: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. · Class II · Potential safety issue with Philips Azurion systems, where longitudinal and transverse table movements may be impacted due to mechanical wear of the Float Tabletop control on the control module.

- 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.