Philips recalls Allura Xper FD20/15 patient tables with catalog number 722058 due to risk of patient falling from 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 all Allura Xper FD20/15 patient tables with catalog number 722058 because the mattress used on the table could cause a patient to fall. This is serious because falls can lead to injuries.
The mattress used on the patient table has a design flaw that can cause the table to tip or shift, increasing the risk of a patient falling. This could result in injuries such as bruises, fractures, or more serious harm.
Healthcare professionals using the Allura Xper FD20/15 patient tables in medical facilities are most at risk. Patients receiving treatment on these tables could fall if the mattress is defective.
Check for the catalog number 722058 on the product label. The recall includes specific serial numbers listed in the official notice.
Look for the catalog number 722058 on the device label to confirm if it is affected.
Philips recalls the Allura Xper FD20/15 patient tables with catalog number 722058 due to a risk of patient falling from the table caused by the mattress design.
Check for the catalog number 722058 on the product label. The recall includes specific serial numbers listed in the official notice.
The recall does not specify a remedy, so affected users should 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-1149-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1149-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
