Philips recalls Allura CV20 patient tables with catalog number 722031 due to possible patient falls from the table. Affected units may need repair or replacement to prevent injury.
Possibility of the patient falling from the table related to the mattress used on the patient table.
Philips is recalling all Allura CV20 patient tables with catalog number 722031 because the mattress used on the table could cause patients to fall. This recall matters because falls can lead to serious injuries.
The mattress used on the patient table has a design flaw that could cause patients to fall from the table during medical procedures. This risk occurs when the mattress does not securely hold the patient's weight.
Healthcare facilities using Philips Allura CV20 patient tables with catalog number 722031 are most at risk. Patients receiving treatment on these tables could fall if the mattress is defective.
Check for the catalog number 722031 on the Allura CV20 patient table. The recall includes all units with this specific catalog number, regardless of serial number.
Look for the catalog number 722031 on the Allura CV20 patient table to confirm if it is affected.
Reach out to Philips Medical Systems Netherlands B.V. to arrange repair or replacement of the affected table.
Philips recalls Allura CV20 patient tables with catalog number 722031 because the mattress used on the table could cause patients to fall.
Check for the catalog number 722031 on the Allura CV20 patient table. The recall includes all units with this specific catalog number.
Contact Philips Medical Systems Netherlands B.V. to arrange repair or replacement of the affected table.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1151-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1151-2025 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.
