# FDA device recall: Philips Azurion, Model Numbers:  722229, 722230, 722231, 722232, 722233, 722234, 722235, and 722236, with Software Versi

> recall · VERIFIED · 2026-07-16

Firm: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. · Class II · Two software related issues:   1) Potential image quality degradation that may lead to delay of therapy, procedural complications and/or inappropriate treatment  and  2) Potential loss of geometry mov

- Company: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Sector: medical devices
- 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.