Philips recalls Allura Xper FD10C system with serial number 722001 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 the Allura Xper FD10C system with serial number 722001 because a finger can get caught between the table's rails during manual repositioning, potentially causing injury to operators and service staff.
During manual repositioning of the patient tabletop, a finger can become trapped between the longitudinal guiding rails and the tabletop. This entrapment could cause finger injury to anyone handling the equipment, including medical staff and service technicians.
Operators and service personnel who use the Allura Xper FD10C system with serial number 722001 are most at risk. This recall affects medical facilities that use this specific model.
Check if your Philips Allura Xper FD10C system has the serial number 722001. This model is part of the Philips Allura and Azurion systems.
Reach out to Philips directly for specific instructions on how to handle the recalled system.
Yes, the recall addresses a risk of finger injury during manual repositioning of the patient table.
Check if your Philips Allura Xper FD10C system has the serial number 722001.
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-1079-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1079-2025 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.
