Philips recalls Azurion 7 B20 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 Azurion 7 B20 systems with three specific serial numbers because during manual patient table repositioning, fingers can get caught between the table's rails. This poses a risk of finger injury to medical staff and service technicians who handle the equipment.
During manual repositioning of the patient table, 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 equipment.
Medical staff and service technicians who operate or maintain the Azurion 7 B20 systems are most at risk. The recall affects specific serial numbers of the Philips medical imaging equipment.
Check for the system codes 722068, 722226, or 722236 on the equipment. The recall applies to Philips Azurion 7 B20 systems sold with these specific serial numbers.
Identify the system code on your Azurion 7 B20 equipment to see if it matches the recalled serial numbers: 722068, 722226, or 722236.
The recall affects Philips Azurion 7 B20 systems with system codes 722068, 722226, and 722236.
During manual repositioning of the patient table, a finger can get trapped between the longitudinal guiding rails and the tabletop, potentially causing finger injury.
The recall does not require immediate stoppage; however, affected users should check the serial numbers and take appropriate action if they have a recalled unit.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1092-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1092-2025 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.
