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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Diagnostic Equipment

Philips Azurion 7M20 FlexArm Systems Recalled for Stand Movement Issues

Agency Publication Date: November 26, 2025
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Summary

Philips Medical Systems Nederland B.V. has recalled 172 units of the Philips Azurion 7M20 systems with FlexArm ceiling-mounted systems (Model Number 722234). The motorized longitudinal movement of the stand may become inconsistent or stop working entirely because grease or oil is leaking from the bearings onto the ceiling rails. This leakage reduces necessary friction and can prevent the stand from moving smoothly or at all during use. Consumers should contact their healthcare provider or the manufacturer to coordinate a repair or correction.

Risk

The excessive lubrication on the ceiling rails causes the motorized stand to move unevenly or fail to move, which could disrupt medical procedures or prevent the proper positioning of imaging equipment during clinical care.

What You Should Do

  1. This recall involves the Philips Azurion 7M20 systems with FlexArm ceiling-mounted system, identified by model number 722234.
  2. Stop using the recalled device immediately.
  3. Contact the manufacturer, Philips Medical Systems Nederland B.V., or your equipment distributor to arrange for a return, replacement, or correction of the system.
  4. Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) for additional questions regarding medical device recalls.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Philips Azurion 7M20 systems with FlexArm ceiling-mounted system
Model / REF:
722234

Expansion to add additional model. Recall #: Z-0719-2026.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97719
Status: Active
Manufacturer: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Sold By: Authorized medical equipment distributors; Direct hospital sales
Manufactured In: Netherlands
Units Affected: 172 units
Distributed To: Alabama, Arkansas, Arizona, California, Colorado, Florida, Georgia, Hawaii, Illinois, Indiana, Kansas, Kentucky, Maryland, Minnesota, Missouri, New Mexico, New York, Ohio, Oklahoma, Pennsylvania, Rhode Island, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia, Wyoming

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.