Philips recalls Allura Xper FD20/10 medical tables due to potential patient falls from the table mattress. Affected units have specific catalog numbers and serial numbers listed in the 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 FD20/10 medical tables because the mattress used on the table could cause patients to fall. This recall affects healthcare facilities that use these tables for medical procedures.
The mattress on the Allura Xper FD20/10 table may not hold securely, increasing the risk of patients falling from the table during medical procedures. This could lead to injuries if the patient slips or the table moves unexpectedly.
Healthcare facilities using Philips Allura Xper FD20/10 tables are most at risk. Patients undergoing procedures on these tables could fall if the mattress is defective.
Check for catalog number 722029 or serial numbers listed in the recall notice. The product is sold under Philips Medical Systems Netherlands B.V. and used in medical facilities.
Look for the serial numbers listed in the recall notice (e.g., 71, 91, 7, etc.) on the table's label or documentation.
Reach out to Philips Medical Systems Netherlands B.V. for guidance on next steps if you have the recalled product.
Philips recalls Allura Xper FD20/10 tables because the mattress used on the table could cause patients to fall during medical procedures.
Check for catalog number 722029 or the specific serial numbers listed in the recall notice (e.g., 71, 91, 7, etc.).
Contact Philips Medical Systems Netherlands B.V. for guidance on next steps if you have the recalled product.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1148-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1148-2025 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.
