Beyond Laser Systems recalls CLUB 1000/2000/4000 laser projectors due to missing manufacturing dates and improper safety labeling, which could lead to unsafe operation.
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.
Beyond Laser Systems is recalling its CLUB 1000, 2000, and 4000 laser light show projectors because they lack required manufacturing dates and safety labels. This could lead to improper operation and potential safety risks if the projectors are used without proper labeling.
The projectors lack required manufacturing dates and safety labels, which could lead to improper operation. The remote interlock connector might not be properly installed or wired, increasing the risk of unsafe laser emissions.
Owners of CLUB 1000, 2000, or 4000 laser projectors manufactured by BLS are affected. Users who rely on these projectors for presentations or home entertainment may be at risk if the safety labels are missing.
Check for projectors labeled with 'CLUB 1000', 'CLUB 2000', or 'CLUB 4000' from Beyond Laser Systems. These models were sold without the required manufacturing date and safety labels.
Look for the model number on the projector to confirm it is a CLUB 1000, 2000, or 4000.
The projectors lack required manufacturing dates and safety labels, which could lead to improper operation and potential safety risks.
Check the model number on the projector to confirm it is a CLUB 1000, 2000, or 4000. The recall does not specify a remedy, so no action is required beyond checking the model.
The recall indicates potential safety risks due to missing labels and improper installation, but no specific injury mechanism is described.
We’ve drafted a message you can send Beyond Laser Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-2112-2025 — Beyond Laser Systems Beyond Laser Systems Hello, I own a Beyond Laser Systems that is covered by recall Z-2112-2025 from Beyond Laser Systems. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
