Beyond Laser Systems recalls DIODE 1000/2000/3000 laser projectors for 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 DIODE 1000/2000/3000 laser projectors because they lack required manufacturing dates and safety labels. This could lead to unsafe operation if the projectors are used without proper identification and safety features.
The projectors have missing manufacturing dates and improper safety labels, which could lead to unsafe operation if the projectors are used without proper identification and safety features. The lack of required labels may prevent users from identifying the correct safety settings and potential hazards.
Users of DIODE 1000/2000/3000 laser projectors manufactured by BLS. Those who have the projectors without proper labeling or manufacturing dates are most at risk.
Check for DIODE 1000/2000/3000 laser projectors with missing manufacturing dates or incomplete safety labels. The projectors were manufactured by BLS and sold under the Beyond Laser Systems brand.
Look for missing manufacturing dates or incomplete safety labels on the projectors.
The projectors lack required manufacturing dates and safety labels, which could lead to unsafe operation.
DIODE 1000/2000/3000 laser projectors manufactured by BLS.
The recall does not provide a fix; users should check for missing labels and dates.
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-2111-2025 — Beyond Laser Systems Beyond Laser Systems Hello, I own a Beyond Laser Systems that is covered by recall Z-2111-2025 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.
