X-Laser Laser Projectors: Laser Safety Risk in Auto/Music Modes
X-Laser recalls Aurora, Caliente Aurora, PSX-400, Mobile Beat Max models due to potential laser safety hazards when used in auto or music modes. Affected users should check their product details.
Use caution until it’s fixed
Failure to comply with performance standard requirements (21 CFR 1040.10(f))when operated in the user accessible auto and music modes of operation
Contact the company
What happened, in plain English
X-Laser is recalling several laser light show projectors because they might not meet safety standards when used in auto or music modes. This could create a risk of injury from the laser light. Read more at govinfonow.com/recall/73371-x-laser-laser-projectors-laser-safety-risk-in-auto-music.
Source Summary by GovInfoNow · govinfonow.com/recall/73371-x-laser-laser-projectors-laser-safety-risk-in-auto-music · Updated September 20, 2026 · FDA enforcement record: FDA #Z-2870-2017
Cite this page
“X-Laser Laser Projectors: Laser Safety Risk in Auto/Music Modes.” GovInfoNow, updated September 20, 2026. https://govinfonow.com/recall/73371-x-laser-laser-projectors-laser-safety-risk-in-auto-music. Based on FDA recall #Z-2870-2017 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2870-2017%22&limit=1).
Why it’s dangerous
The projectors may not meet safety standards when operated in auto or music modes. This could cause the laser light to be unsafe for users, potentially leading to injury.
Who’s affected
Users of X-Laser laser projectors like Aurora, Caliente Aurora, PSX-400, Mobile Beat Max, and Mobile Beat Max MKII models are affected. People using these devices in auto or music modes are most at risk.
How to tell if you have this one
Check for the model names: Aurora, Caliente Aurora, PSX-400, Mobile Beat Max, Mobile Beat Max MKII, X-Beam, or Hawk 500. These are the affected X-Laser laser light show projectors.
- Brand
X-Laser- Category
Medical device
What to do — step by step
Check Product Model
Identify your X-Laser laser projector model from the list: Aurora, Caliente Aurora, PSX-400, Mobile Beat Max, Mobile Beat Max MKII, X-Beam, or Hawk 500.
How this recall unfolded
Recall timeline
FDA terminated this recall 6.7 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-2870-2017 (July 24, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2870-2017 to see it in context.
- Plain-language summary written by qwen3:4b on September 20, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.