X-Laser Laser Light Show projector models Aurora — Class II medical device recall Z-2870-2017
Terminated recall by X-Laser Llc, reported 2017-09-20. Failure to comply with performance standard requirements (21 CFR 1040.10(f))when operated in the user accessib
| Recall number | Z-2870-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | FDA mandated |
| Recalling firm | X-Laser Llc, Laurel, MD, United States |
| Recall initiated | 2017-07-24 |
| Classified | 2017-09-13 |
| Reported by FDA | 2017-09-20 |
| Terminated | 2024-04-16 |
| Quantity | 830 |
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.
Reason for recall
Failure to comply with performance standard requirements (21 CFR 1040.10(f))when operated in the user accessible auto and music modes of operation
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2870-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.