Philips recalls Azurion 7 B20 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 B20 medical imaging systems with model numbers 722068, 722226, and 722236. The recall is because the table may move unexpectedly when the Reset Geometry button is pressed, even when 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 movement could lead to injury to patients or staff during medical procedures if the table shifts suddenly.
Medical facilities using Philips Azurion 7 B20 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 if your system has model numbers 722068, 722226, or 722236. Also verify the software version starts with R1.X, R2.X, or R3.X. The serial number is listed as 'All' in the recall notice.
Identify your system model number from the label on the device, which should be one of 722068, 722226, or 722236.
Confirm your software version starts with R1.X, R2.X, or R3.X to determine if it is affected.
Yes, if your Philips Azurion 7 B20 system has model numbers 722068, 722226, or 722236 and software versions starting with R1.X, R2.X, or R3.X.
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-1347-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1347-2026 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.
