Philips recalls Azurion 3 M15 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 3 M15 medical imaging systems with model numbers 722064, 722222, 722230, and 722280 (for OUS only) because pressing the Reset Geometry button can cause the table to move unexpectedly even when a table lock is active. This could lead to potential injury during medical procedures.
Pressing the Reset Geometry button on the system can cause the table to move unexpectedly even when the table lock is engaged. This could happen under certain conditions, potentially leading to injury during medical procedures if the table shifts unexpectedly.
Medical facilities using Philips Azurion 3 M15 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 for model numbers 722064, 722222, 722230, or 722280 (for OUS only) on the system. The software version is R1.X, R2.X, or R3.X. All systems with these model numbers and software versions are affected.
Identify the model number on your system to confirm if it is one of the recalled numbers: 722064, 722222, 722230, or 722280 (for OUS only).
Ensure your software version is R1.X, R2.X, or R3.X to confirm it is affected by this recall.
No, only systems with specific model numbers (722064, 722222, 722230, 722280 for OUS only) and software versions R1.X, R2.X, or R3.X are affected.
The recall record does not specify a remedy, so no action is required beyond checking if your system is affected.
Yes, the recall states that pressing this button can cause the table to move unexpectedly even with the table lock engaged, which could lead to injury during medical procedures.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1345-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1345-2026 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.
