Class II

Medical Device Recall: Zenition 50; Product Number (REF): 718096; Interventional fluoroscopic x-ray system

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. · September 29, 2025

Reason for Recall

Over time some systems may experience loss of imaging functionality and/or poor image quality due to potential corrosion of the Image Intensifier Television (IITV) control board.

Distribution

Distribution US states of MO and TX; Belgium, Canada, Fiji, Germany, India, Malaysia, Mexico, Morocco, South Africa, South Korea, Thailand, United Kingdom, and Uzbekistan.

States Affected

MO, TX

Quantity Affected

29 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0241-2026

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: Zenition 50; Product Number (REF): 718096; Interventional fluoroscopic x-ray system | SafeCheck