Philips recalls Azurion 7 B12 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 7 B12 systems with model numbers 722067, 722225, and 722235 and all software versions R1.X, R2.X, R3.X. The table may move unexpectedly when the Reset Geometry button is pressed, even when a table lock is active. This could lead to injury if the table moves during medical procedures.
Pressing the Reset Geometry button can cause the table to move unexpectedly, even when the table lock is engaged. This movement could lead to injury during medical procedures if the table shifts while a patient is being treated.
Medical facilities using the Azurion 7 B12 system with the listed model numbers and software versions are most at risk. Patients undergoing procedures with this equipment could be affected if the table moves unexpectedly.
Check the model numbers: 722067, 722225, or 722235. Verify the software version is R1.X, R2.X, or R3.X. The system may also have specific UDI-DIs listed in the recall notice.
Identify if your system has model numbers 722067, 722225, or 722235.
Confirm the software version is R1.X, R2.X, or R3.X.
This recall affects Azurion 7 B12 systems with model numbers 722067, 722225, or 722235 and software versions R1.X, R2.X, or R3.X. If your system matches these, you are affected.
The recall does not specify a remedy, so contact Philips directly for guidance on next steps.
Yes, the recall states that the table may move unexpectedly when the Reset Geometry button is pressed, even when a table lock is active.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1346-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1346-2026 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.
