# FDA device recall: Integris-Allura system; System Code Description (Model Numbers): Integris CV Cesar-Powerpack-Visub-Nicol (722030), Integ

> recall · VERIFIED · 2026-04-28

Firm: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. · Class II · The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leakage may affect the co

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

---
Source: MedFuel Intel news monitor. Verification tier: VERIFIED.