Gk Photonics recalls ClubMax Laser Projectors due to insufficient safety interlock preventing laser radiation exposure. Users must replace the remote interlock dongle to prevent injury.
The User Remote Interlock Dongle provided with the E-Stop Remote is not sufficient to fully comply with the FDA's Manual Reset Mechanism requirement for laser projectors and could unintentionally expose the user and/or observers to high power laser radiation. It needs to be replaced for safety reasons.
Gk Photon: ClubMax Laser Projectors are recalled because the safety interlock dongle doesn't meet FDA laser safety standards, potentially exposing users to harmful laser radiation. This requires replacing the dongle to prevent injury.
The remote interlock dongle doesn't fully comply with FDA safety requirements for laser projectors. This means the device could unintentionally expose users and observers to high-power laser radiation during normal operation.
Owners of ClubMax Laser Projectors with the E-Stop Remote are affected. Users most at risk are those who operate the projectors without replacing the interlock dongle.
Check if your ClubMax Laser Projector has the E-Stop Remote. The recall applies to all ClubMax Laser Projection Series products.
Remove the existing E-Stop Remote interlock dongle and install a compliant replacement as specified by the manufacturer.
The User Remote Interlock Dongle provided with the E-Stop Remote does not fully comply with FDA's Manual Reset Mechanism requirements for laser projectors, potentially exposing users to harmful laser radiation.
No, but you must replace the interlock dongle to ensure safety. Continuing to use without replacement could pose a risk.
All ClubMax Laser Projection Series products with the E-Stop Remote are affected by this recall.
We’ve drafted a message you can send Gk Photonics to request your refund or repair — edit it as you like.
Subject: Recall Z-2092-2019 — Gk Photonics Gk Photonics Hello, I own a Gk Photonics that is covered by recall Z-2092-2019 from Gk Photonics. 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.
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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.
