Philips recalls Allura Xper FD10/10 patient tables with specific catalog numbers due to potential patient falls from the table. Affected units may need inspection or replacement.
Possibility of the patient falling from the table related to the mattress used on the patient table.
Philips is recalling Allura Xper FD10/10 patient tables with catalog numbers 722005, 722011, and 722027 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 patient table might not be securely attached, increasing the risk of patients falling from the table during medical procedures. This could lead to injuries if the table is not properly stabilized.
Healthcare facilities using the Allura Xper FD10/10 patient tables with the specified catalog numbers are most at risk. Patients receiving treatment on these tables could be affected if the mattress fails.
Check for catalog numbers 722005, 722011, or 722027 on the Allura Xper FD10/10 patient tables. Serial numbers are listed in the recall notice for verification.
Look for the catalog numbers 722005, 722011, or 722027 on the patient table to confirm if it is affected.
Philips recalls Allura Xper FD10/10 patient tables with specific catalog numbers because the mattress used on the table could cause patients to fall during medical procedures.
Check for catalog numbers 722005, 722011, or 722027 on the Allura Xper FD10/10 patient table. Serial numbers are listed in the recall notice for verification.
The recall notice does not specify a remedy or action steps for affected tables. Contact Philips for further guidance.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1143-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1143-2025 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.
