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.