Philips recalls Allura Xper FD10 systems with ADN7NT patient tables (model 722010, software 8.1.100) due to risk of unintended table movement after software update. Affected units may require repair or replacement.
When Software upgrade 8.1.100 is installed on an Allura Xper with an AD7NT (non tilt) table, the pivot brake does not engage. This issue may cause unexpected movements of the table.
Philips is recalling Allura Xper FD10 systems with specific ADN7NT patient tables that may move unexpectedly after a software update. This could lead to patient safety risks if the table shifts during medical procedures.
The software update 8.1.100 causes the pivot brake on the ADN7NT table to fail to engage. This means the table might move unexpectedly during medical procedures, potentially causing injury to patients or staff.
Healthcare facilities using Philips Allura Xper FD10 systems with ADN7NT patient tables (model 722010, software version 8.1.100) are most at risk. Patients undergoing procedures with these systems could be affected if the table moves unexpectedly.
Check for model number 722010 and software version 8.1.100 on the Philips Allura Xper FD10 system with an ADN7NT patient table. Serial numbers 774, 909, or 526 are also associated with this recall.
Verify the software version on your Philips Allura Xper FD10 system with ADN7NT table. If it is 8.1.100, it is affected.
Reach out to Philips for guidance on whether your system needs repair or replacement.
The software update 8.1.100 causes the pivot brake on the ADN7NT table to fail, which may lead to unexpected table movement during medical procedures.
Check for model number 722010 and software version 8.1.100 on the Philips Allura Xper FD10 system with an ADN7NT patient table. Serial numbers 774, 909, or 526 are also affected.
Contact Philips directly for instructions on repair or replacement, as the recall does not specify immediate action.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1896-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1896-2024 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.
