FDAJuly 24, 2017device
X-Laser Laser Light Show projector models Aurora, Caliente Aurora, PSX-400, Mobile Beat Max, Mobile Beat Max MKII, X-Beam, Hawk 500 High-power laser light show projector.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Failure to comply with performance standard requirements (21 CFR 1040.10(f))when operated in the user accessible auto and music modes of operation
What to do
FDA enforcement status: Terminated
Brands named
x laser
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDALaser light show projectors manufactured by BLS, Model PURE 5000/10000.2025-06-30
- FDALaser light show projectors manufactured by BLS, Model CLUB 1000/2000/4000.2025-06-30
- FDALaser light show projectors manufactured by BLS, Model DIODE 1000/2000/3000.2025-06-30
- FDAFusion Pro 24, Model 170002024-08-08
- FDAClass IV New Era medical laser device2020-01-29
- FDABeijing Syntech Laser UL C02 Laser surgical lasers2017-07-03
- FDABeijing Syntech Laser Trixel C02 Laser surgical lasers2017-07-03
- FDABeijing Syntech Laser Diode Laser surgical lasers2017-07-03
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