⚠ RecallRadar📷 ScanGuidesOfficial U.S. recall notices, restated plainly

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Zenition 50; Product Number (REF): 718096; Interventional fluoroscopic x-ray system

Medical DevicesSource: FDA (device) · Date: 2025-10-29

Read the official notice at FDA (device) →

Share on XFacebookRedditEmail

Get alerts for Philips Medical Systems Nederland B.v

Guides: Which agency handles which recall (FDA vs USDA vs CPSC vs NHTSA)

The text below is copied from the official FDA (device) record. If anything differs, the official notice is correct.

Company / brand
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Product
Zenition 50; Product Number (REF): 718096; Interventional fluoroscopic x-ray system
Reason / hazard
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.
Classification
Class II
Status
Ongoing
Distribution / sold at
Distribution US states of MO and TX; Belgium, Canada, Fiji, Germany, India, Malaysia, Mexico, Morocco, South Africa, South Korea, Thailand, United Kingdom, and Uzbekistan.
Recall initiated
2025-09-29
Code info
Product Number (REF): 718096; UDI-DI: 00884838091535; All serial numbers;
Product quantity
29 units
Voluntary mandated
Voluntary: Firm initiated
City
Best
Country
Netherlands
Event id
97682
Free daily digest + "My products" watchlist

Get the daily digest, and tell us what to watch. Everything is optional except your email.

Free allergen alerts:

Categories:

Privacy: we store only what you enter here, use it only to send recall alerts you asked for, never sell or share it, and you can unsubscribe anytime. Double opt-in: we will email you a confirmation link before sending anything; alerts start only after you confirm. Every email has unsubscribe and manage-watchlist links.