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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

Beyond Laser Systems Laser Projectors Recalled for Safety Interlock Defects

Agency Publication Date: July 16, 2025
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Summary

Beyond Laser Systems, LLC is recalling approximately 25 laser light show projectors from their DIODE, CLUB, and PURE model families. These high-power Class IV lasers are missing a required safety interlock feature, or have safety components that were installed but never actually wired to work. The devices also lack required safety labels, including manufacture dates and certification info, and the manufacturer failed to provide specific user manuals for each model or test the manual reset function for emergency shutdowns.

Risk

The remote safety stop is either missing or non-functional, meaning the laser cannot be shut down quickly during an emergency. This poses a risk of accidental exposure to dangerous laser radiation, which can cause permanent eye damage or skin burns.

What You Should Do

  1. This recall affects Beyond Laser Systems (BLS) laser light show projectors including model families DIODE (1000, 2000, 3000), CLUB (1000, 2000, 4000), and PURE (5000, 10000).
  2. Stop using the recalled laser projectors immediately.
  3. Contact Beyond Laser Systems, LLC to arrange for a repair, replacement, or correction to ensure the safety interlocks and labeling are properly installed.
  4. Call the FDA Consumer Complaint hotline at 1-888-463-6332 or visit www.fda.gov/medical-devices/medical-device-recalls for additional information.

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: Laser light show projectors, Model DIODE 1000/2000/3000
Model / REF:
DIODE 1000
DIODE 2000
DIODE 3000

Recall #: Z-2111-2025

Product: Laser light show projectors, Model CLUB 1000/2000/4000
Model / REF:
CLUB 1000
CLUB 2000
CLUB 4000

Recall #: Z-2112-2025

Product: Laser light show projectors, Model PURE 5000/10000
Model / REF:
PURE 5000
PURE 10000

Recall #: Z-2113-2025

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97176
Status: Active
Manufacturer: Beyond Laser Systems, LLC
Manufactured In: United States
Units Affected: 3 products (10; 12; 3)
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.