Philips recalls Cardio Vascular-Allura Centron model 722400 (OUS only) due to fall risk from patient table mattress. Affected units have specific serial numbers.
Possibility of the patient falling from the table related to the mattress used on the patient table.
Philips is recalling a specific model of medical table (Cardio Vascular-Allura Centron) because the mattress used on it could cause patients to fall. This is a serious hazard that requires immediate attention to prevent injury.
The mattress on the patient table has a design flaw that could cause patients to fall from the table during medical procedures. This fall risk is serious and could lead to injury.
Healthcare facilities using the recalled model in the U.S. are affected. Patients on the table during use are at risk of falling.
Check if your medical table has the model name 'Cardio Vascular-Allura Centron' and catalog number 722400. The serial numbers listed in the recall include specific numbers like 531, 314, 432, and others.
Immediately stop using the Cardio Vascular-Allura Centron model 722400 if you have it, as it poses a fall risk to patients.
No, this recall applies only to the U.S. Overseas (OUS) market.
The catalog number is 722400.
Check the serial number against the list provided in the recall: 531, 314, 432, 376, 496, and other specific numbers.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1161-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1161-2025 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.
