Philips recalls Allura Xper FD20 OR Tables with catalog numbers 722023 and 722035 due to potential patient falls from the table. Affected units may need repair or replacement.
Possibility of the patient falling from the table related to the mattress used on the patient table.
Philips is recalling Allura Xper FD20 OR Tables with specific catalog numbers because the mattress used on the table could cause patients to fall. This recall matters because falls can lead to serious injuries during medical procedures.
The mattress on the patient table could allow patients to fall during procedures. This fall risk is due to the table's design or the mattress's stability, which may not hold patients securely.
Patients undergoing medical procedures using the Allura Xper FD20 OR Table are most at risk. Healthcare facilities that own or use these tables may also be affected.
Check for catalog numbers 722023 or 722035 on the table. The table may also have serial numbers 175 or 208.
Look for catalog numbers 722023 or 722035 on the table's label.
Reach out to Philips directly for instructions on whether the table needs repair or replacement.
The recall is due to a possibility of patients falling from the table related to the mattress used on the table.
Catalog numbers 722023 and 722035 are affected.
The recall does not require immediate stop use; contact Philips for guidance 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-1147-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1147-2025 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.
