Beyond Laser Systems, LLC: Device Recall

Recall #Z-2112-2025 · 06/30/2025

Class II: Risk

Recall Details

Recall Number
Z-2112-2025
Classification
Class II
Product Type
Device
Recalling Firm
Beyond Laser Systems, LLC
Status
Ongoing
Date Initiated
06/30/2025
Location
Austin, TX, United States
Voluntary/Mandated
FDA Mandated
Product Quantity
12

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 emission from Class IV laser projectors after an interruption caused using a remote interlock. No supplemental product reports, as required according to 21 CFR 1002.11.

Product Description

Laser light show projectors manufactured by BLS, Model CLUB 1000/2000/4000.

Distribution Pattern

US Nationwide Distribution

Other Recalls by Beyond Laser Systems, LLC

View all recalls by Beyond Laser Systems, LLC →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.