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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/Monitoring Devices

Skytron Freedom 4FXS-60 Monitor Mounts Recalled for Falling Hazard

Agency Publication Date: April 23, 2025
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Summary

IHB OPERATIONS B.V. has recalled 112 units of the Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount because the provided mounting hardware does not screw in deeply enough to support the weight of the monitor. This defect can cause the mounting hardware to fail, leading to the monitor frame separating and falling from its column. No injuries have been reported, but owners should immediately stop using the mount and contact their Skytron distributor for a resolution.

Risk

The monitor and frame can unexpectedly detach and fall from the mounting column. This poses a serious impact injury risk to any patients or healthcare staff positioned beneath or near the device.

What You Should Do

  1. The recalled products are Skytron Freedom 4FXS-60 Heavy Duty Monitor Mounts with UDI/DI 10841736116071. All serial numbers are affected by this recall.
  2. Stop using the recalled monitor mount immediately to prevent the device from falling.
  3. Contact your Skytron authorized distributor or IHB OPERATIONS B.V. directly to arrange for a return, replacement, or corrective repair of the mounting hardware.
  4. Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) if you have 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: Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount
Model / REF:
4FXS-60
Serial Numbers:
All Serial Numbers
UDI:
10841736116071

Recall number Z-1663-2025.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96581
Status: Active
Manufacturer: IHB OPERATIONS B.V.
Sold By: Skytron authorized distributors
Manufactured In: Netherlands
Units Affected: 112 units
Distributed To: Alabama, Arizona, California, Florida, Iowa, Idaho, Illinois, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, North Carolina, New Hampshire, New Jersey, New Mexico, New York, Pennsylvania, Tennessee, Texas, Utah, Virginia, Wisconsin, West Virginia

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.