Philips recalls AlluraXper FD20 Biplane OR Table Systems with serial numbers 722020 and 722025 due to risk of finger entrapment during patient 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 Biplane OR Table Systems with serial numbers 722020 and 722025. The recall is because during manual patient repositioning, fingers can get trapped between the tabletop and guiding rails, potentially causing injury to operators or service personnel.
During manual repositioning of the patient tabletop, fingers can get trapped between the longitudinal guiding rails and the tabletop. This entrapment may cause finger injury to operators or service personnel who handle the equipment.
Users of the Philips AlluraXper FD20 Biplane OR Table System with serial numbers 722020 or 722025 are affected. Operators and service personnel who manually reposition patients are most at risk.
Check for serial numbers 722020 or 722025 on the Philips AlluraXper FD20 Biplane OR Table System. The product was sold under the Philips brand.
Reach out to Philips directly for specific guidance on the recall and next steps.
During manual repositioning of the patient tabletop, fingers can get trapped between the longitudinal guiding rails and the tabletop, potentially causing finger injury.
Serial numbers 722020 and 722025.
Check for serial numbers 722020 or 722025 on the Philips AlluraXper FD20 Biplane OR Table System.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1082-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1082-2025 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.
