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Open, Classified

Burstberry Laser Projection Series

FDA Recall Z-2097-2019 · Posted None

Recalling FirmGk Photonics Inc
Recall StatusOpen, Classified
Product CodeREA
Date Initiated2019-07-10

Reason for Recall

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.

Root Cause

Radiation Control for Health and Safety Act

Distribution Pattern

Unknown

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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