Philips recalls Azurion 3 M12 medical tables with catalog numbers 722063 and 722221 due to possible 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 3 M12 medical tables with specific catalog numbers because the mattress used on the table could cause patients to fall. This is serious as falls could lead to injuries.
The mattress used on the patient table may not hold securely, increasing the risk of patients falling from the table during medical procedures. This could cause injuries such as bruises or fractures.
Healthcare providers using Philips Azurion 3 M12 tables with catalog numbers 722063 or 722221 are affected. Patients at risk include those receiving procedures on these tables.
Check for catalog numbers 722063 or 722221 on the Azurion 3 M12 table. The recall was issued for specific models sold in the U.S. and Canada.
Look for catalog numbers 722063 or 722221 on the Azurion 3 M12 table to confirm if it is recalled.
The recall is due to a possibility of patients falling from the table caused by the mattress used on the Azurion 3 M12 table.
Check the catalog number on the table. If it is 722063 or 722221, contact Philips for further instructions.
Yes, the hazard could cause patients to fall, which might lead to injuries such as bruises or fractures.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1153-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1153-2025 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.
