Philips recalls AlluraXperFD20/15 patient tables with system code 722058 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 AlluraXperFD20/15 patient tables with system code 722058 because during manual repositioning, fingers can get trapped between the tabletop and guiding rails, potentially causing injury. This risk applies to medical staff 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 operators and service personnel who handle the equipment.
Medical staff and service personnel who operate or maintain Philips AlluraXperFD20/15 patient tables with system code 722058 are most at risk of finger injury during manual repositioning.
Check for the system code 722058 on your Philips AlluraXperFD20/15 patient table. The product was sold with UDI: 00884838059115(21).
Look for the system code 722058 on your Philips AlluraXperFD20/15 patient table.
During manual repositioning of the patient tabletop, fingers can get trapped between the longitudinal guiding rails and the tabletop, potentially causing finger injury.
Medical staff and service personnel who operate or maintain the Philips AlluraXperFD20/15 patient tables.
Check for the system code 722058 on your Philips AlluraXperFD20/15 patient table. The product was sold with UDI: 00884838059115(21).
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1086-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1086-2025 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.
