Philips recalls Allura Xper FD20/20 patient tables with catalog number 722038 due to risk of patient falling 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 all Allura Xper FD20/20 patient tables with catalog number 722038 because the mattress used on the table could cause patients to fall. This is serious as falls can lead to injuries.
The mattress used on the patient table may not be securely attached, increasing the risk of patients falling from the table during medical procedures. This could lead to injuries such as bruises, fractures, or more serious harm.
Healthcare facilities using Philips Allura Xper FD20/20 patient tables with catalog number 722038 are most at risk. Patients during medical procedures could fall if the table's mattress is defective.
Check for catalog number 722038 on the product label. The recall includes specific serial numbers listed in the official notice.
Look for catalog number 722038 on the product label to confirm if your table is affected.
Reach out to Philips Medical Systems Netherlands B.V. for instructions on repair or replacement.
The mattress used on the table may not be securely attached, increasing the risk of patients falling during medical procedures.
Check for catalog number 722038 on the product label and contact Philips Medical Systems Netherlands B.V. for repair or replacement instructions.
Yes, patients could fall from the table during procedures, potentially causing injuries like bruises, fractures, or more serious harm.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1150-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1150-2025 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.
