# FDA recall Z-2113-2025

> **Beyond Laser Systems, LLC** · Class II · device recall initiated 2025-06-30.

## Product

Laser light show projectors manufactured by BLS, Model PURE 5000/10000.

## Reason for recall

The remote interlock connector, which is required by 21 CFR 1040.10(f)(3), in the remote stop box was not installed the connector or was mechanically installed but not wired. The labels placed on the projectors do not meet requirements specified in 21 CFR 1010.4 (Variances), 21 CFR 1010.2 (Certification), 21 CFR 1010.3 (Identification) and 21 CFR 1040.10 (g)(Labelling requirements). The identification label does not include the date of manufacture as required by 21 CFR 1010.3.  The corrective action plan covers three families of laser light show of projectors: DIODE. CLUB and PURE with three different hardware configurations such as the number of the number of  RJ45 ports, radiant power of emissions and network configurations. No specific user manuals were provided to each model family as required by 21 CFR 1040.10(h)(1) (Informational requirements   (1) User information). The Quality Control test did not validate the manual reset function to enable resumption of laser radiation emissi

## Distribution

US Nationwide Distribution

## Key facts

- **Recall number:** Z-2113-2025
- **Recalling firm:** Beyond Laser Systems, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-06-30
- **Report date:** 2025-07-23

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Austin, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2113-2025

## Citation

> AI Analytics. FDA recall Z-2113-2025. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-2113-2025. Source: US FDA. Licensed CC0.

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