Beyond Laser Systems recalls PURE 5000/10000 laser projectors due to missing manufacturer date labels and improper remote interlock connectors, which could cause safety issues.
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 their PURE 5000/10000 laser projectors because they lack required manufacturer date labels and have faulty remote interlock connectors. This defect could lead to safety risks if the projectors are used without proper labeling or correct wiring.
The projectors have missing manufacturer date labels and improperly installed remote interlock connectors. This could lead to safety issues if the projectors are used without proper labeling or correct wiring, potentially causing hazards like unintended laser activation.
Owners of PURE 5000/10000 laser projectors manufactured by Beyond Laser Systems are affected. Users with these projectors may face safety risks due to improper labeling and faulty connectors.
Check for laser projectors labeled 'PURE 5000' or 'PURE 10000' made by Beyond Laser Systems. The product does not have a manufacturer date label as required by safety regulations.
Look for the missing manufacturer date label on the projector.
The projectors lack required manufacturer date labels and have improperly installed remote interlock connectors, which could cause safety issues.
Check for the missing manufacturer date label and ensure the remote interlock connector is properly installed and wired.
The recall record does not mention any corrective actions or fixes.
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-2113-2025 — Beyond Laser Systems Beyond Laser Systems Hello, I own a Beyond Laser Systems that is covered by recall Z-2113-2025 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.
