Philips recalls AlluraXper FD10/10 patient tables with serial numbers 722005, 722011, and 722027 due to risk of finger entrapment during patient repositioning. Owners should stop using affected units immediately.
Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel
Philips is recalling AlluraXper FD10/10 patient tables with specific serial numbers because during manual patient repositioning, fingers can get trapped between the tabletop and guiding rails. This could cause finger injuries for medical staff and service personnel who handle the equipment.
During manual repositioning of the patient tabletop, a finger can become trapped between the longitudinal guiding rails and the tabletop. This entrapment could cause finger injuries for operators and service personnel who handle the equipment.
Medical staff and service personnel who use the Philips AlluraXper FD10/10 patient tables with serial numbers 722005, 722011, or 722027 are most at risk of finger injury during patient repositioning.
Check if your Philips AlluraXper FD10/10 patient table has serial numbers 722005, 722011, or 722027. The product was sold with specific UDI codes listed in the recall notice.
Discontinue use of the affected patient table as it poses a risk of finger injury during repositioning.
All Philips AlluraXper FD10/10 patient tables with serial numbers 722005, 722011, or 722027.
Check for the serial numbers 722005, 722011, or 722027 on your Philips AlluraXper FD10/10 patient table.
Stop using the table immediately to prevent finger injury during patient repositioning.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1078-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1078-2025 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.
