Philips recalls Azurion Interventional Fluoroscopic X-ray Systems with software versions R1.0, R1.1, or R1.2 due to potential loss of X-ray imaging functionality and longer cold restart times.
Potential Loss of Imaging (X-ray) Functionality and/or Longer Time to Perform Cold Restart
Philips is recalling certain Azurion Interventional Fluoroscopic X-ray Systems with specific software versions. These systems may lose X-ray imaging functionality or take longer to restart, which could affect medical procedures.
The software versions R1.0, R1.1, and R1.2 may cause the X-ray system to lose imaging functionality or take longer to restart. This could lead to delays in medical procedures or incomplete imaging during surgeries.
Healthcare facilities using Philips Azurion systems with software versions R1.0, R1.1, or R1.2 are most at risk. Patients undergoing procedures with these systems may experience delays or imaging issues.
Check for model numbers 722063, 722064, 722067, 722068, 722078, or 722079 with software versions R1.0, R1.1, or R1.2. These systems are used for medical procedures like vascular and neuro surgeries.
Verify the software version on your Philips Azurion system to see if it is R1.0, R1.1, or R1.2.
Reach out to Philips for guidance on whether your system needs an update or repair.
Software versions R1.0, R1.1, and R1.2.
Check for model numbers 722063, 722064, 722067, 722068, 722078, or 722079 with software versions R1.0, R1.1, or R1.2.
No, but you should check the software version and contact Philips for updates or repairs.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2534-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-2534-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.