Gk Photonics recalls Atom Laser Projection Series projectors due to insufficient safety interlock dongles risking laser radiation exposure. Users must replace the dongle to prevent unintended high-power laser exposure.
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 Atom Laser Projection Series projectors because the included User Remote Interlock Dongle doesn't meet FDA safety standards for laser projectors. This could expose users and observers to harmful laser radiation if not fixed.
The User Remote Interlock Dongle doesn't fully comply with FDA requirements for laser projectors. This means the device might unintentionally expose users and observers to high-power laser radiation during normal operation.
Users of Atom Laser Projection Series projectors who have the included User Remote Interlock Dongle are affected. Those using the projectors without proper safety interlocks are at higher risk.
Check for the Atom Laser Projection Series product name on the device. The recall applies to all units sold by Gk Photonics that came with the User Remote Interlock Dongle.
Remove the current User Remote Interlock Dongle and install a compliant one to meet FDA safety standards.
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, which could expose users and observers to high-power laser radiation.
No, but you must replace the User Remote Interlock Dongle to ensure safety compliance with FDA standards.
Check if your Atom Laser Projection Series product came with the User Remote Interlock Dongle. All units sold by Gk Photonics are affected.
We’ve drafted a message you can send Gk Photonics to request your refund or repair — edit it as you like.
Subject: Recall Z-2093-2019 — Gk Photonics Gk Photonics Hello, I own a Gk Photonics that is covered by recall Z-2093-2019 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.
