Class II — X-Laser Llc
| Recalling firm | A.R.C. Laser GmbH |
|---|---|
| Registered facility | A.R.C. LASER GMBH (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Failure to comply with performance standard requirements (21 CFR 1040.10(f))when operated in the user accessible auto and music modes of operation |
| Product | 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. |
| Quantity | 830 |
| Distribution | US Distribution |
| Initiated | 2017-07-24 |
| Classified | 2017-09-13 |
| Terminated | 2024-04-16 |
| Recall number | Z-2870-2017 |
| Initiation | FDA Mandated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — X-Laser Llc (Z-2870-2017).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/77843/
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