Philips recalls Allura Xper FD10C patient tables due to fall risk from mattress design. Affected units have catalog number 722001. No remedy specified in recall notice.
Possibility of the patient falling from the table related to the mattress used on the patient table.
Philips is recalling all Allura Xper FD10C patient tables because the mattress design could cause patients to fall from the table. This is a safety issue that requires immediate attention to prevent injuries.
The mattress used on the patient table has a design that could allow patients to fall from the table during procedures. This hazard occurs when the table's stability is compromised by the mattress structure.
Healthcare facilities using Philips Allura Xper FD10C patient tables with catalog number 722001 are affected. Patients at risk include those receiving treatment on these tables.
Check for the catalog number 722001 on the Allura Xper FD10C patient table. The recall covers all units with this specific catalog number.
Look for the catalog number 722001 on the patient table to confirm if it's affected.
The recall notice does not specify any remedy or fix for this issue.
Check for the catalog number 722001 on the Allura Xper FD10C patient table.
The recall notice does not provide specific action steps for affected units.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1152-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1152-2025 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.
