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Gk Photonics Inc recalls Maxim Laser Projection Series
Recalled August 14, 2019 · FDA recall Z-2095-2019 · Gk Photonics
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. · FDA Class II
Units
N/A
Sold at
Unknown
Description
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.
Product
Maxim Laser Projection Series
Manufacturer(s)
Gk Photonics Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →