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Open, Classified

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

FDA Recall Z-2112-2025 · Posted 2025-07-16

Recall StatusOpen, Classified
Product CodeREA
Date Initiated2025-06-30
Product Quantity12

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.

Firm Action

Beyond Laser Systems (BLS) mail the CAP letters to all affected customers. BLS will complete the procedure and ship the laser projector back to the customer within 14-21 days of receiving the units in our facility. BLS will provide a UPS shipping label to the customer for shipping to our facility and cover the expense of shipping the units back to the customer via UPS. If you have any questions, call 512-220-9339 ext 302.

Root Cause

Radiation Control for Health and Safety Act

Distribution Pattern

US Nationwide Distribution

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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