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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
Other/Industrial & Commercial

Bodor I Series Laser Cutting Machines Recalled for Safety Standard Violations

Agency Publication Date: July 23, 2025
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Summary

Jinan Bodor Cnc Machine Co Ltd is recalling 20 of its Bodor I series laser cutting machines because they fail to meet federal safety standards for light-emitting products. This recall was mandated by the FDA because the devices do not comply with specific performance standards for laser products. Consumers should stop using the machines immediately and contact the manufacturer to arrange for a safety correction or return.

Risk

The machines fail to meet federal laser safety standards, which may result in users being exposed to hazardous laser radiation. This can cause severe and permanent injury to the eyes and skin during operation or maintenance.

What You Should Do

  1. This recall involves Bodor I series laser cutting machines, which are identified by Accession Number 2421628- 001.
  2. Stop using the recalled laser cutting machine immediately.
  3. Contact Jinan Bodor Cnc Machine Co Ltd or your distributor to arrange for a return, replacement, or safety correction of the device.
  4. Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) for additional questions regarding this recall.

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: Bodor I series laser cutting machine
Model / REF:
I Series

The Accession Number is 2421628- 001. Recall number Z-2149-2025.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97284
Status: Active
Manufacturer: Jinan Bodor Cnc Machine Co Ltd
Sold By: Authorized distributors
Manufactured In: China
Units Affected: 20
Distributed To: Nationwide

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.