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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 P and C Series Laser Cutting Machines Recalled for Laser Non-Compliance

Agency Publication Date: January 18, 2025
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Summary

Jinan Bodor Cnc Machine Co Ltd has recalled 269 units of its Bodor P and C series laser cutting machines because they are non-compliant with federal laser product safety standards. The recall affects P series units with code 2421537-000 and C series units with code 2421612-000. While no injuries have been reported to date, the machines were found to have defects that do not meet regulatory requirements for laser products. Consumers should stop using the machines and contact the manufacturer or their distributor to arrange for a correction or return.

Risk

The laser systems in these machines do not comply with safety performance standards, which can result in unintended exposure to hazardous laser radiation. This exposure poses a moderate risk of serious eye or skin injuries to operators and bystanders.

What You Should Do

  1. The recalled products are Bodor P and C series laser cutting machines. Affected P series units are identified by code 2421537-000, and C series units are identified by code 2421612-000.
  2. Stop using the recalled equipment immediately to prevent potential exposure to hazardous laser radiation.
  3. Contact Jinan Bodor Cnc Machine Co Ltd or your authorized industrial equipment distributor to arrange for a return, replacement, or a safety correction to bring the machine into compliance.
  4. Call the FDA at 1-888-463-6332 for additional information or to report any safety concerns regarding these devices.

Your Remedy Options

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

Affected Products

Product: Bodor P series laser cutting machines
Model / REF:
2421537-000

P series identifier from code information.

Product: Bodor C series laser cutting machines
Model / REF:
2421612-000

C series identifier from code information.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96035
Status: Active
Manufacturer: Jinan Bodor Cnc Machine Co Ltd
Sold By: Authorized industrial equipment distributors
Manufactured In: China
Units Affected: 269 units
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.