# FDA recall Z-2870-2017

> **X-Laser Llc** · Class II · device recall initiated 2017-07-24.

## 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

## Distribution

US Distribution

## Key facts

- **Recall number:** Z-2870-2017
- **Recalling firm:** X-Laser Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-07-24
- **Report date:** 2017-09-20
- **Termination date:** 2024-04-16

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Laurel, MD, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2870-2017

## Citation

> AI Analytics. FDA recall Z-2870-2017. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-2870-2017. Source: US FDA. Licensed CC0.

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