Philips recalls Azurion 5 M20 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 specific Azurion 5 M20 systems with serial numbers 722228, 722232, and 722281. The risk comes from fingers getting caught between the table's guiding rails and tabletop during manual patient repositioning, which could cause finger injury to medical staff.
During manual repositioning of the patient tabletop, fingers can become trapped between the longitudinal guiding rails and the tabletop. This entrapment could cause finger injury to medical staff and service personnel who handle the equipment.
Medical staff and service personnel who use the Azurion 5 M20 systems with the listed serial numbers are most at risk. The hazard applies specifically to operators during manual patient table repositioning.
Check for the system code numbers 722228, 722232, or 722281 on the device. The serial numbers are also listed in the UDI (Unique Device Identification) codes provided in the recall notice.
Identify the system code on your Azurion 5 M20 device to confirm if it matches the recalled serial numbers: 722228, 722232, or 722281.
The affected models are Philips Azurion 5 M20 systems with system codes 722228, 722232, and 722281.
Check the system code on your device; if it matches 722228, 722232, or 722281, it is affected.
The recall record does not specify a remedy, so no action is required beyond checking if your device is affected.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1090-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1090-2025 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.
