Philips recalls Allura Xper FD20 Biplane OR Table models with catalog numbers 722020 and 722025 due to potential patient falls from the table. Affected units may need inspection or correction.
Possibility of the patient falling from the table related to the mattress used on the patient table.
Philips is recalling Allura Xper FD20 Biplane or Table models with specific catalog numbers because the mattress used on the table could cause patients to fall. This is a safety issue that needs attention to prevent injuries.
The mattress on the patient table could allow patients to fall if not properly secured. This risk exists during medical procedures where patients are positioned on the table.
Patients undergoing medical procedures using this equipment are most at risk. Healthcare facilities that own or use these devices may be affected.
Check for catalog numbers 722020 or 722025 on the device. The serial numbers may be 6 digits or 2-3 digits.
Identify the catalog number on the device to confirm if it is affected.
The recall states there is a possibility of patient falling from the table, which could lead to injury. However, the exact risk level is not specified in the notice.
Look for catalog numbers 722020 or 722025 on the device. Serial numbers may be 6 digits or 2-3 digits.
The recall does not specify a remedy, so contact Philips directly 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-1146-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1146-2025 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.
