Philips recalls Zenition 50 interventional fluoroscopic x-ray systems with product number 718096 due to potential corrosion causing image quality problems. Affected units may need repair or replacement.
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.
Philips is recalling its Zenition 50 interventional fluoroscopic x-ray systems (product number 718096) because corrosion of the Image Intensifier Television control board can lead to loss of imaging functionality or poor image quality. This affects medical facilities using the equipment for procedures like angiography.
Corrosion of the Image Intensifier Television control board over time can cause the x-ray system to lose imaging functionality or produce poor image quality. This may lead to inaccurate diagnostic images during medical procedures.
Medical facilities that use the Zenition 50 x-ray system for procedures such as angiography are most likely affected. Patients undergoing these procedures may experience reduced image quality due to the system malfunction.
Check for the product number 718096 on the Zenition 50 x-ray system. The system was sold with a unique device identifier (UDI-DI) starting with 00884838091535. All serial numbers are listed in the recall notice.
Verify if your Zenition 50 x-ray system has the product number 718096 or the UDI-DI starting with 00884838091535.
The recall affects medical facilities using the system, which may impact patients during procedures. However, the hazard is not directly dangerous to patients in normal use.
Check for the product number 718096 or the UDI-DI starting with 00884838091535 on your Zenition 50 x-ray system.
The recall notice does not specify a remedy, so contact Philips directly for guidance on next steps.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0241-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-0241-2026 from Philips. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
