Philips recalls Azurion 5 M20 systems with specific model numbers and software versions due to risk of unexpected table movement when pressing Reset Geometry button, even with lock engaged.
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
Philips is recalling Azurion 5 M20 medical imaging systems with model numbers 722228, 722232, and 722281 (for OUS only) and all software versions R1.X, R2.X, R3.X. The recall is because the table might move unexpectedly when the Reset Geometry button is pressed, even if a table lock is active.
Pressing the Reset Geometry button can cause the table to move unexpectedly, even when the table lock is engaged. This could lead to potential injuries if the table shifts during medical procedures.
Medical facilities using Philips Azurion 5 M20 systems with the listed model numbers and software versions are affected. Staff and patients using these systems during procedures are at risk if the table moves unexpectedly.
Check your Azurion 5 M20 system's model number (722228, 722232, or 722281 for OUS only) and software version (R1.X, R2.X, or R3.X). The system may also have specific serial numbers or UDI-DIs listed in the recall notice.
Verify your Azurion 5 M20 system's model number and software version to confirm if it is in the recall list.
Reach out to Philips Medical Systems Netherlands for guidance on next steps and potential fixes.
The table may move unexpectedly when the Reset Geometry button is pressed, even with the table lock active, which could lead to injuries during medical procedures.
Model numbers 722228, 722232, and 722281 (for OUS only) with software versions R1.X, R2.X, or R3.X.
No, but you should check if your system is affected and contact Philips 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-1351-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1351-2026 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.
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.
