Philips recalls Azurion 5 M12 systems with specific serial numbers due to risk of finger entrapment between table rails during patient 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 Azurion 5 M12 systems with serial numbers 722227 and 722231 because repositioning the patient table could trap a finger between the rails, potentially 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 become trapped 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 technicians who operate or maintain Philips Azurion 5 M12 systems with the specific serial numbers listed are most at risk. Patients are not directly affected by this recall.
Check for Azurion 5 M12 systems with serial numbers 722227 or 722231. The unique device identifiers (UDIs) for these units are listed in the recall notice.
Verify if your Azurion 5 M12 system has serial numbers 722227 or 722231.
During manual repositioning of the patient tabletop, a finger can get trapped between the longitudinal guiding rails and the tabletop, potentially causing finger injury to operators and service personnel.
Check for Azurion 5 M12 systems with serial numbers 722227 or 722231. The unique device identifiers (UDIs) for these units are listed in the recall notice.
No, patients are not affected by this recall. The hazard applies only to operators and service personnel who handle the equipment.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1089-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1089-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
