Philips recalls Azurion 7M20 systems with FlexArm ceiling mounts due to inconsistent motor movement from grease leakage causing lubrication issues. Affected models include 722234.
The motorized longitudinal movement of the FlexArm stand may be inconsistent (not smooth) and eventually may become unavailable. This issue is due to grease leakage from the bearings and/or anti-corrosion oil applied on the bearings, because of which the lubrication on the ceiling rail may be excessive, reducing the friction between the rails and the friction wheel. Expansion to add additional model.
Philips is recalling Azurion 7M20 systems with FlexArm ceiling-mounted systems because the motor movement may become inconsistent and stop working due to grease leakage. This could affect medical imaging equipment in hospitals and clinics.
Grease leakage from the bearings causes excessive lubrication on the ceiling rail, reducing friction between the rails and the friction wheel. This makes the motorized movement inconsistent and may eventually stop working.
Hospitals and clinics using Philips Azurion 7M20 systems with FlexArm ceiling mounts are most affected. The risk is low for users as the issue is unlikely to cause immediate harm.
Check for the model number 722234 on Philips Azurion 7M20 systems with FlexArm ceiling-mounted systems. This recall applies to specific medical imaging equipment sold in the U.S.
Look for the model number 722234 on the system's label or documentation.
The motorized movement of the FlexArm stand may become inconsistent and stop working due to grease leakage from bearings causing excessive lubrication.
This is a low-risk issue that may cause inconsistent movement over time but does not pose an immediate risk of injury or damage.
Check the model number on your system; if it's 722234, contact Philips for more information.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0719-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-0719-2026 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.
