Philips recalls Allura Xper FD20 systems with ADN7NT patient tables and software version 8.1.100 due to pivot brake failure risk. Affected units may experience unexpected table movements.
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 FD20 systems with specific ADN7NT patient tables and software version 8.1.100. The software update can cause the pivot brake to fail, potentially leading to unexpected table movements during medical procedures.
When software version 8.1.100 is installed on an Allura Xper system with an ADN7NT table, the pivot brake fails to engage. This can cause the table to move unexpectedly during patient treatment, potentially causing injury.
Healthcare facilities using Philips Allura Xper FD20 systems with ADN7NT patient tables and software version 8.1.100 are most at risk. Patients and staff during medical procedures may be affected if the table moves unexpectedly.
Check for model number 722012 and software version 8.1.100 on the Allura Xper FD20 system with an ADN7NT patient table. The serial number is 2138 for affected units.
Verify the software version on your Allura Xper FD20 system; affected units have version 8.1.100.
Reach out to Philips for guidance on the recall and potential remedies.
The model number is 722012 for the Allura Xper FD20 system with an ADN7NT patient table.
Software version 8.1.100 is the affected version.
Check for model number 722012 and software version 8.1.100 on your Allura Xper FD20 system with an ADN7NT patient table.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1895-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1895-2024 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.
