Philips recalls AlluraXper FD20 systems with specific serial numbers due to risk of finger entrapment during patient table repositioning. Affected users should contact Philips for details.
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 FD20 patient tables with three specific serial numbers because repositioning the tabletop can trap a finger between the rails and table, potentially causing injury. This hazard affects medical staff and service personnel who handle the equipment.
During manual repositioning of the patient tabletop, a finger can get stuck between the longitudinal guiding rails and the tabletop. This entrapment can cause finger injury to operators and service personnel who handle the equipment.
Medical staff and service personnel who operate or maintain Philips AlluraXper FD20 patient tables with the recalled serial numbers are most at risk. Patients are not directly affected by this hazard.
Check if your AlluraXper FD20 system has serial numbers 722006, 722012, or 722028. The unique device identifier (UDI) codes are listed in the recall notice for verification.
Reach out to Philips directly to confirm if your specific AlluraXper FD20 system is affected by the recall.
During manual repositioning of the patient tabletop, a finger can get trapped between the longitudinal guiding rails and the tabletop, potentially causing injury to operators and service personnel.
The affected serial numbers are 722006, 722012, and 722028 for the AlluraXper FD20 system.
No, patients are not directly affected by this hazard. The recall applies to medical staff and service personnel who operate or maintain the equipment.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1080-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1080-2025 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.
