Gk Photonics Inc Spectrum Laser Projection Series Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Spectrum Laser Projection Series
Brand
Gk Photonics Inc
Lot Codes / Batch Numbers
Spectrum Laser Projection Series
Products Sold
Spectrum Laser Projection Series
Gk Photonics Inc is recalling Spectrum Laser Projection Series due to 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 f. Based on FDA medical device recall database.
Summary derived from FDA notice
The following details were not provided by the FDA: corrective action details.
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
Healthcare providers and patients should stop using the device and contact the manufacturer for further instructions. Report problems to FDA MedWatch.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026