Philips recalls Allura Xper FD20 Biplane models with specific catalog numbers due to potential patient falls from the table. Learn how to identify affected units and what to do.
Possibility of the patient falling from the table related to the mattress used on the patient table.
Philips is recalling all Allura Xper FD20 Biplane models with catalog numbers 722008 and 722013 because the patient table mattress could cause patients to fall. This is a safety issue that requires immediate attention to prevent injuries.
The mattress used on the patient table has a design flaw that could cause patients to fall from the table during medical procedures. This risk exists when the table is in normal use without additional safety measures.
Healthcare professionals using the Allura Xper FD20 Biplane for medical procedures are most at risk. Patients undergoing treatments on this equipment could fall if the mattress is defective.
Check for catalog numbers 722008 or 722013 on the device. Serial numbers are listed in the recall notice, but specific numbers are not provided for general users.
Look for catalog numbers 722008 or 722013 on the Allura Xper FD20 Biplane device.
This recall applies to Philips Allura Xper FD20 Biplane models with catalog numbers 722008 or 722013. If your device has these numbers, it is affected.
Check for catalog numbers 722008 or 722013 on the device. Serial numbers are listed in the recall notice but specific numbers are not provided for general users.
The recall does not specify a remedy, so contact Philips directly to determine next steps for affected devices.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1145-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1145-2025 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.
