FDAJune 30, 2025device

Laser light show projectors manufactured by BLS, Model DIODE 1000/2000/3000.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Ongoing

Brands named

beyond laser systemsbeyondbeyond laser

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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