Philips recalls Allura Xper FD10 patient tables with serial numbers 722003-722026 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 Allura Xper FD10 patient tables with specific serial numbers because during manual patient repositioning, fingers can get trapped between the tabletop and guiding rails. This could cause finger injuries to operators and service personnel.
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 injuries to medical staff handling the equipment.
Operators and service personnel who use Philips Allura Xper FD10 patient tables with serial numbers 722003, 722010, or 722026 are most at risk. These tables are used in medical settings for patient repositioning.
Check if your Philips Allura Xper FD10 table has serial numbers 722003, 722010, or 722026. The unique device identifier (UDI) codes are listed in the recall notice.
Reach out to Philips Medical Systems Netherlands B.V. for specific instructions on how to handle the recalled tables.
Allura Xper FD10 patient tables with serial numbers 722003, 722010, or 722026.
Check the serial number on your table; affected models have serial numbers 722003, 722010, or 722026.
Contact Philips Medical Systems Netherlands B.V. for specific instructions on handling the recalled tables.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1077-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1077-2025 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.
