Philips recalls Azurion 5 M12 patient tables with catalog numbers 722227 and 722231 (OUS only) due to possible patient falls from the table mattress.
Possibility of the patient falling from the table related to the mattress used on the patient table.
Philips is recalling Azurion 5 M12 medical tables with specific catalog numbers (722227 and 722231) sold only in overseas markets. The recall is because the mattress used on these tables might cause patients to fall.
The mattress on the Azurion 5 M12 table might not hold securely, increasing the risk of patients falling from the table during medical procedures. This could lead to injuries if the patient loses balance.
Healthcare facilities using Philips Azurion 5 M12 tables with catalog numbers 722227 or 722231 (sold only overseas) are most at risk. Patients using these tables could fall if the mattress is defective.
Check for catalog numbers 722227 or 722231 on the table's label. These models were sold only in overseas markets (OUS) and have specific serial numbers listed in the recall notice.
Look for catalog numbers 722227 or 722231 on the table's label to confirm if it's affected.
Reach out to Philips customer support for guidance on next steps if the table is affected.
Philips recalls these tables because the mattress used on the Azurion 5 M12 might cause patients to fall during medical procedures.
No, these specific models (catalog numbers 722227 and 722231) were only sold in overseas markets (OUS).
Check the table's label for catalog numbers 722227 or 722231. If affected, contact Philips customer support for guidance.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1155-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1155-2025 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.
