Philips recalls AlluraXper FD20 Biplane systems with serial numbers 722008 and 722013 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 specific AlluraXper FD20 Biplane systems that could trap a finger between the tabletop and guiding rails during manual patient repositioning. This poses a risk of finger injury to operators and service personnel.
During manual repositioning of the patient tabletop, a finger can get caught between the longitudinal guiding rails and the tabletop. This entrapment may cause finger injury to operators and service personnel who handle the equipment.
Medical professionals and service technicians who use the AlluraXper FD20 Biplane system with serial numbers 722008 or 722013 are most at risk. The hazard applies during manual repositioning of the patient tabletop.
Check for the system code numbers 722008 or 722013 on the AlluraXper FD20 Biplane system. The recall covers specific units sold with these serial numbers.
Identify the system code on your AlluraXper FD20 Biplane system to confirm if it matches 722008 or 722013.
During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop, potentially causing finger injury.
Check for system code numbers 722008 or 722013 on your AlluraXper FD20 Biplane system.
The recall does not specify a remedy, but Philips may provide guidance on how to address the hazard.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1081-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1081-2025 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.
