Philips recalls AlluraXperFD20/10 patient tables with system code 722029 due to finger entrapment risk during manual repositioning. Affected units may cause finger injury to operators and service personnel.
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 AlluraXperFD20/10 patient tables with system code 722029 because during manual repositioning, fingers can get trapped between the tabletop and guiding rails, potentially causing injury. This risk applies to operators and service personnel who handle the equipment.
During manual repositioning of the patient tabletop, fingers can become trapped between the longitudinal guiding rails and the tabletop. This entrapment may cause finger injury to individuals handling the equipment. The hazard occurs only during specific manual movements and not during normal operation.
Operators and service personnel who use or maintain Philips AlluraXperFD20/10 patient tables are most at risk. The recall affects specific system codes produced by Philips Medical Systems Netherlands B.V.
Check for system code 722029 on the AlluraXperFD20/10 patient tables. The recall applies to units sold with this specific system code.
Verify the system code on your AlluraXperFD20/10 patient table; affected units have system code 722029.
Yes, during manual repositioning, fingers can get trapped between the tabletop and guiding rails, potentially causing finger injury to operators and service personnel.
Check for system code 722029 on your AlluraXperFD20/10 patient table; affected units have this specific code.
The recall does not specify a remedy, so contact Philips Medical Systems Netherlands B.V. for guidance on next steps.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1084-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1084-2025 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.
