Gk Photonics recalls Maxim Laser Projection Series projectors due to insufficient user remote interlock dongle that could expose users to high power laser radiation. Replace the dongle for safety.
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:ics recalls Maxim Laser Projection Series projectors because the included user remote interlock dongle doesn't meet safety standards and could expose users to harmful laser radiation. This is a safety issue that needs fixing to prevent injury.
The user remote interlock dongle in the E-Stop Remote doesn't fully meet FDA safety standards for laser projectors. This could allow the laser to activate unintentionally, exposing users and observers to high power laser radiation that can cause eye damage or skin injury.
Users of Maxim Laser Projection Series projectors who have the E-Stop Remote with the included user remote interlock dongle are most at risk. This affects anyone using these projectors for presentations or home entertainment.
Check if your Maxim Laser Projection Series projector has the E-Stop Remote with a user remote interlock dongle. The product was sold by Gk Photonics Inc and is part of the Maxim Laser Projection Series line.
Remove the current user remote interlock dongle and install a compliant replacement to meet safety standards.
No, only those with the E-Stop Remote that includes the user remote interlock dongle.
Check if your Maxim Laser Projection Series projector has the E-Stop Remote with the included user remote interlock dongle.
Replace the user remote interlock dongle with a compliant one to meet safety standards.
We’ve drafted a message you can send Gk Photonics to request your refund or repair — edit it as you like.
Subject: Recall Z-2095-2019 — Gk Photonics Gk Photonics Hello, I own a Gk Photonics that is covered by recall Z-2095-2019 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.
