Philips recalls Azurion 3 M12 systems with specific model numbers and software versions due to risk of unexpected table movement when pressing the 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 3 M12 medical imaging systems with model numbers 722063, 722221, and 722229. The recall is because the table might move unexpectedly when the Reset Geometry button is pressed, even if a table lock is active. This could cause injury during medical procedures.
Pressing the Reset Geometry button can cause the table to move unexpectedly, even when the table lock is engaged. This could lead to injuries such as falls or collisions during medical procedures. The hazard occurs under specific conditions that may not be obvious to users.
Medical facilities using Philips Azurion 3 M12 systems with the listed model numbers and software versions are most at risk. Patients and staff during imaging procedures could be affected if the table moves unexpectedly.
Check for model numbers 722063, 722221, or 722229 on the system. The software version is R1.X, R2.X, or R3.X. The recall applies to all units with these model numbers and software versions.
Identify the model numbers on your system: 722063, 722221, or 722229.
Ensure the software version is R1.X, R2.X, or R3.X.
This recall applies to Philips Azurion 3 M12 systems with model numbers 722063, 722221, or 722229 and software versions R1.X, R2.X, or R3.X.
Check your system model and software version. If they match the recalled items, contact Philips for further instructions.
The recall does not require immediate stoppage, but you should avoid pressing the Reset Geometry button without ensuring the table is stable.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1344-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1344-2026 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.
