FDAJuly 10, 2019device
Spectrum Laser Projection Series
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
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.
What to do
FDA enforcement status: Ongoing
Brands named
gk photonics
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDAWasatch Photonics 785/830-SR and 785-ER-ILC Raman Spectrometers, Product Models: 785-SR-ILP, 785-SR-ILC, 830-SR-ILP, 830-SR-ILC,785-ER-ILC.2025-08-04
- FDAMaxim Laser Projection Series2019-07-10
- FDALogolas Laser Projection Series2019-07-10
- FDAAtom Laser Projection Series2019-07-10
- FDAClubMax Laser Projection Series2019-07-10
- FDABurstberry Laser Projection Series2019-07-10
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