Philips recalls Azurion 3 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 specific Azur:ion 3 M12 systems with serial numbers 722063 and 722221. The recall is because during manual patient table repositioning, fingers can get trapped between the table's rails, 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 can cause finger injury to operators and service personnel who handle the system.
Operators and service personnel who use the Azurion 3 M12 system with serial numbers 722063 or 722221 are most at risk. These individuals may experience finger injury if they reposition the patient table manually.
Check for the Azurion 3 M12 system with serial numbers 722063 or 722221. The system code is listed in the recall notice as (1) 722063 and (2) 722221.
Look for the system code on the device: 722063 or 722221.
Reach out to Philips directly for specific instructions on how to safely handle the device or if a fix is needed.
The Philips Azurion 3 M12 system with serial numbers 722063 and 722221 is being recalled.
Check the system code on your device; affected units have serial numbers 722063 or 722221.
The recall record does not specify a remedy, so contact Philips directly for guidance.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1087-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1087-2025 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.
