Philips recalls AlluraXper FD20 OR Table systems with serial numbers 722023 and 722035 due to finger entrapment risk 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 OR Table systems with specific serial numbers because repositioning the patient table could trap a finger between the rails, causing injury. This risk applies to 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 could cause finger injury to operators and service personnel who handle the equipment.
Medical staff and service personnel who use the Philips AlluraXper FD20 OR Table systems are most at risk. The recall affects specific serial numbers sold in the U.S. market.
Check for the AlluraXper FD20 OR Table system with serial numbers 722023 or 722035. The product was sold in the U.S. under Philips Medical Systems Netherlands B.V.
Reach out to Philips Medical Systems Netherlands B.V. for specific instructions on the recall.
During manual repositioning of the patient tabletop, a finger can get trapped between the longitudinal guiding rails and the tabletop, potentially causing finger injury.
Serial numbers 722023 and 722035 for the AlluraXper FD20 OR Table system.
The recall does not require immediate stop-use; contact Philips for specific instructions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1083-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1083-2025 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.
