Philips recalls Azurion 3 M15 systems with specific serial numbers due to risk of finger entrapment during patient table repositioning. Affected units may cause 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 3 M15 medical imaging systems with three specific serial numbers. The recall is because during manual repositioning of the patient table, fingers can get trapped between the table and guiding rails, potentially causing injury to medical 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 injury to the finger, particularly for medical staff and service personnel who operate the system.
Medical staff and service personnel who use the Azurion 3 M15 systems with the listed serial numbers are most at risk. The hazard applies specifically to operators handling the patient tables during manual repositioning.
Check if your Azurion 3 M15 system has one of the serial numbers: 722064, 722222, or 722280. The UDI codes are also listed in the recall notice for identification.
Identify your Azurion 3 M15 system's serial number to see if it matches the recalled numbers: 722064, 722222, or 722280.
Reach out to Philips directly for specific instructions on how to safely handle the system or if a fix is needed.
The affected models are Philips Azurion 3 M15 systems with serial numbers 722064, 722222, or 722280.
Check your system's serial number against the recalled numbers: 722064, 722222, or 722280. The UDI codes are also listed in the recall notice.
The recall record does not specify a remedy or fix for this issue.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1088-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1088-2025 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.
