Philips recalls Allura Xper FD20 medical imaging tables with catalog numbers 722006, 722012, and 722028 due to possible patient falls from the table mattress.
Possibility of the patient falling from the table related to the mattress used on the patient table.
Philips is recalling Allura Xper FD20 medical imaging tables with specific catalog numbers because the mattress used on the table could cause patients to fall. This is a safety issue that requires attention to prevent injuries.
The mattress used on the Allura Xper FD20 table may not stay securely attached to the table, which could lead to patients falling from the table during medical procedures. This hazard is related to the table's design and how the mattress is attached.
Medical facilities that own or use the Allura Xper FD20 imaging tables with catalog numbers 722006, 722012, or 722028 are most at risk. Patients using these tables could fall if the mattress is not properly secured.
Check your Allura Xper FD20 table for catalog numbers 722006, 722012, or 722028. The product may also have specific serial numbers listed in the recall notice.
Look for catalog numbers 722006, 722012, or 722028 on the product label.
Reach out to Philips Medical Systems Netherlands B.V. for further assistance or to confirm if your table is affected.
The recall is for potential patient falls from the table mattress, which could lead to injury. However, the hazard is not described as causing death or serious injury in normal use.
Check for catalog numbers 722006, 722012, or 722028 on your Allura Xper FD20 table. The product may also have specific serial numbers listed in the recall notice.
Contact Philips Medical Systems Netherlands B.V. to confirm if your table is affected and to get instructions on next steps.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1144-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1144-2025 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.
