Philips recalls Azurion Interventional Fluoroscopy systems with software version 2.1.x (model numbers 722063-722228) due to risk of table lock-up when pressing both APC and Float Tabletop buttons simultaneously, potentially causing imaging unavailability.
When the user presses or releases both the APC (accept) button and the Float Tabletop (panning) button at the same time, the geometry may stop reacting on movement requests (table lock-up) and X-ray imaging becomes unavailable.
Philips is recalling certain Azurion Interventional Fluoroscopy systems with software version 2.1.x (model numbers 722063-722228) because pressing both the APC and Float Tabletop buttons at the same time can cause the table to lock up and stop X-ray imaging. This could lead to incomplete procedures or delays in medical treatments.
When the user presses or releases both the APC (accept) button and the Float Tabletop (panning) button at the same time, the system may lock the table in place. This prevents the X-ray imaging from functioning properly during procedures, potentially causing incomplete treatments or delays.
Healthcare professionals using Philips Azurion Interventional Fluoroscopy systems with software version 2.1.x (model numbers 722063-722228) are affected. The risk is highest for medical staff operating these systems during procedures where precise table movement is critical.
Check if your Philips Azurion Interventional Fluoroscopy system has software version 2.1.x and model numbers 722063, 722064, 722067, 722068, 722078, 722079, 722221, 722222, 722223, 722224, 722225, 722226, 722227, or 722228. The system also has a unique device identifier (UDI#) listed in the serial numbers provided.
Verify your system's software version by checking the device settings or documentation; the affected version is 2.1.x.
Philips will provide a software update to fix the issue; contact Philips support for instructions on how to update.
The affected models are 722063, 722064, 722067, 722068, 722078, 722079, 722221, 722222, 722223, 722224, 722225, 722226, 722227, and 722228.
Check your system's software version in the device settings or documentation; the affected version is 2.1.x.
Contact Philips support to update the software to the latest version to resolve the table lock-up issue.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0213-2022 — Philips Philips Hello, I own a Philips that is covered by recall Z-0213-2022 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.
