Philips recalls Azurion 5 M20 patient tables with catalog numbers 722228, 722232 (OUS only), and 722281 (OUS only) due to potential patient falls from the table.
Possibility of the patient falling from the table related to the mattress used on the patient table.
Philips is recalling Azurion 5 M20 medical tables that could cause patients to fall from the table due to the mattress design. This is a safety issue for healthcare facilities using these tables.
The mattress used on the patient table may not hold securely, increasing the risk of patients falling during medical procedures. This could lead to injuries if the patient falls from the table.
Healthcare facilities that own or use Philips Azurion 5 M20 tables with the specified catalog numbers are most at risk. Patients could fall if the table is used improperly.
Check for catalog numbers: 722228, 722232 (only sold outside the U.S.), or 722281 (only sold outside the U.S.). The product is a medical table used in healthcare settings.
Identify the catalog number on the table's label to confirm if it's in the recalled list: 722228, 722232 (OUS only), or 722281 (OUS only).
Reach out to Philips directly for specific instructions on whether the table needs repair or replacement.
Philips recalls Azurion 5 M20 tables due to a potential risk of patients falling from the table caused by the mattress design.
No, but healthcare facilities should check if their table is in the recall list and contact Philips for guidance on next steps.
Look for catalog numbers 722228, 722232 (only sold outside the U.S.), or 722281 (only sold outside the U.S.) on the table's label.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1156-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1156-2025 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.
