FDASeptember 29, 2025device

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

Official recall recorded by the U.S. Food & Drug Administration.

The 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.

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems nederland b vphilipsphilips medical

UPCs

00884838091535

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Zenition 50; Product Number (REF): 718096; Interventional fluoroscopic x-ray system — Recall Details · AllClear