Z-2095-2019 Class II Ongoing
Recall Details
- Product Type
- Devices
- Report Date
- August 14, 2019
- Initiation Date
- July 10, 2019
- Termination Date
- N/A
- Voluntary/Mandated
- FDA Mandated
- Product Quantity
- N/A
Product Description
Maxim Laser Projection Series
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.
Distribution Pattern
Unknown
Code Information
Maxim Laser Projection Series