Philips recalls Azurion 7 M12 systems with specific serial numbers due to risk of finger entrapment during patient table 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 M12 system models because during manual patient table repositioning, fingers can get trapped between the tabletop and guiding rails, potentially causing injury. This risk applies to healthcare workers 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 may cause finger injury to operators and service personnel who handle the equipment.
Healthcare workers and service technicians who use the Azurion 7 M12 systems are most at risk. The recall affects specific serial numbers of the system.
Check for system codes 722078, 722223, or 722233 on the Azurion 7 M12 system. The recall applies to specific units with unique identifiers listed in the official notice.
Identify the system code on your Azurion 7 M12 system to confirm if it matches the recalled serial numbers: 722078, 722223, or 722233.
During manual repositioning of the patient tabletop, a finger can get trapped between the longitudinal guiding rails and the tabletop, potentially causing finger injury.
Check for system codes 722078, 722223, or 722233 on your Azurion 7 M12 system. The recall applies to specific units with unique identifiers listed in the official notice.
The recall does not specify a remedy, so affected users should contact Philips directly for guidance on next steps.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1093-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1093-2025 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.
