Gk Photonics recalls Spectrum 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 Photonics is recalling Spectrum Laser Projection Series projectors because the included user remote interlock dongle doesn't meet FDA safety standards for laser projectors. This could unintentionally expose users to harmful laser radiation if the dongle fails.
The user remote interlock dongle doesn't fully comply with FDA requirements for laser projectors. If the dongle fails, it could allow high-power laser radiation to reach users or observers without proper safety mechanisms.
Users of Spectrum Laser Projection Series projectors who have the included user remote interlock dongle are affected. Those who use the projectors for presentations or home entertainment are most at risk.
Check if your projector is part of the Spectrum Laser Projection Series. The issue involves the user remote interlock dongle included with the E-Stop Remote.
Remove the current user remote interlock dongle and install a compliant replacement as specified by the manufacturer.
The user remote interlock dongle does not fully comply with FDA safety requirements for laser projectors, which could expose users to high-power laser radiation.
No, you can continue using the projector but must replace the user remote interlock dongle to ensure safety.
Check if your projector is part of the Spectrum Laser Projection Series and includes the user remote interlock dongle with the E-Stop Remote.
We’ve drafted a message you can send Gk Photonics to request your refund or repair — edit it as you like.
Subject: Recall Z-2094-2019 — Gk Photonics Gk Photonics Hello, I own a Gk Photonics that is covered by recall Z-2094-2019 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.
