Class II

Medical Device Recall: Philips Allura, Cardio Vascular-Allura Centron. Model Number: 722400. Interventional Fluoroscopic X-Ray System.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. · June 17, 2026

Reason for Recall

Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.

Distribution

US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

257 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2893-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Medical Device Recall: Philips Allura, Cardio Vascular-Allura Centron. Model Number: 722400. Interventional Fluoroscopic X-Ray System. | SafeCheck