Reported Oct 29, 2025 · Ongoing

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

Philips Medical Systems Nederland B.v.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. · Veenpluis 4-6 · Best · N/A

Is this the product you have?

  • Zenition 50
  • Product Number (REF)718096; Interventional fluoroscopic x-ray system
Lot codes and dates
  • Product Number (REF)718096
  • UDI-DI00884838091535; All serial numbers
Amount recalled
29 units

Where it was sold

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:21 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.