Philips recalls Azurion 7 M20 system models with specific serial numbers due to risk of finger entrapment between patient table rails during manual repositioning. Affected users should contact Philips for details.
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 Azurion 7 M20 system models because during manual patient table repositioning, fingers can get trapped between the table and guiding rails, potentially causing injury. This risk applies to operators and service personnel who handle the equipment.
During manual repositioning of the patient table, fingers can become trapped between the longitudinal guiding rails and the tabletop. This entrapment may cause finger injury, particularly for individuals who frequently adjust the table position.
Operators and service personnel who use the Azurion 7 M20 system with the listed serial numbers are most at risk. The recall affects medical devices used in hospitals and clinics.
Check the system code on the device label for serial numbers 722224, 722079, 722234, or 722282 (with specific UDI codes). The recall applies to Azurion 7 M20 systems sold in the U.S. between 2021 and 2022.
Look for the system code on the device label to confirm if your Azurion 7 M20 system is affected.
Reach out to Philips directly for instructions on how to proceed with the recall.
The affected models are Azurion 7 M20 systems with system codes 722224, 722079, 722234, 722282, and 722078, 722223, 722233.
Check the system code on the device label for the listed serial numbers. The recall applies to Azurion 7 M20 systems sold in the U.S. between 2021 and 2022.
No, the recall requires contacting Philips for instructions, but immediate use is not dangerous.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1094-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1094-2025 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.
