Philips recalls Allura Xper FD20/20 systems with serial number 722038 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 Allura Xper FD20/20 systems with specific serial numbers because moving the patient table could trap a finger between the rails, causing injury. This risk applies to medical staff and service technicians 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 can cause finger injury to operators and service personnel who handle the equipment.
Medical staff and service technicians who use the Philips Allura Xper FD20/20 system with serial number 722038 are most at risk. The recall affects users who manually reposition the patient table.
Check for the system code 722038 on the Allura Xper FD20/20 system. The recall applies to specific models sold with this serial number.
Reach out to Philips directly for specific instructions on how to handle the recalled system.
Yes, it can cause finger injury during manual repositioning of the patient table.
Check for the system code 722038 on your Allura Xper FD20/20 system.
Contact Philips directly for specific instructions on handling the recalled system.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1085-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1085-2025 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.
