Philips recalls Azurion Interventional Fluoroscopic X-ray Systems with specific disk bay models due to potential system failure during procedures. Affected units include Azurion 3 M12, M15, 5 M20, and 7 B12/B20/M12/M20 models with listed serial numbers.
Disk Bay may not perform as intended. System may stop functioning and imaging may not be possible, resulting in delay of procedure.
Philips is recalling specific models of Azurion Interventional Fluoroscopic X-ray Systems because the disk bay may not function properly, which could delay medical procedures. This issue affects certain versions of the system used in hospitals and clinics.
The disk bay component may fail to perform its intended function, causing the system to stop working and preventing imaging during medical procedures. This could lead to delays in critical treatments but does not pose a direct risk of injury to users.
Healthcare facilities using the affected Philips Azurion X-ray systems are most at risk. Patients undergoing procedures with these systems may experience delays but no immediate safety hazards.
Check if your system is listed in the affected models: Azurion 3 M12, M15, 5 M20, or 7 B12/B20/M12/M20 with specific serial numbers provided in the recall notice.
Identify your Philips Azurion system model and serial number to confirm if it's affected by this recall.
Reach out to Philips customer support for assistance with the recall process if your system is listed.
No, the recall does not pose a direct safety risk to patients. The issue may cause procedure delays but does not involve injury or health hazards.
Affected models include Azurion 3 M12, M15, 5 M20, 7 B12, B20, M12, and M20 with specific serial numbers listed in the recall notice.
No, the recall does not require immediate discontinuation of use. Healthcare facilities can continue using the system but should check for the affected models and contact Philips for guidance.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1152-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1152-2024 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.
