Philips recalls Azurion 7 B12 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 three specific Azurion 7 B12 systems with serial numbers 722067, 722225, and 722235. The recall is because during manual patient table repositioning, fingers can get trapped between the table's rails, potentially causing finger injuries to medical staff.
During manual repositioning of the patient table, fingers can become trapped between the longitudinal guiding rails and the tabletop. This entrapment can cause finger injuries to operators and service personnel who handle the equipment.
Medical staff and service personnel who operate or maintain the Azurion 7 B12 systems with the listed serial numbers are most at risk. Patients are not affected by this recall.
Check if your Azurion 7 B12 system has one of the serial numbers: 722067, 722225, or 722235. The system code is listed on the device or in the product documentation.
Identify the system code on your Azurion 7 B12 device to see if it matches the recalled serial numbers: 722067, 722225, or 722235.
During manual repositioning of the patient tabletop, fingers can get trapped between the longitudinal guiding rails and the tabletop, potentially causing finger injuries to operators and service personnel.
No, patients do not use these systems. The recall affects only medical staff and service personnel who operate or maintain the equipment.
Check the system code on your Azurion 7 B12 device; affected units have serial numbers 722067, 722225, or 722235.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1091-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1091-2025 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.
