Fusion Pro 24 Laser (Epilog) - Interlock Device Placement (2024)
Incorrectly placed interlock can expose users to dangerous laser radiation.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Fusion Pro 24, Model 17000
Brand
Epilog Laser Corp.
Lot Codes / Batch Numbers
Model 17000 Product Report Accession Number: 2021046-000
Products Sold
Model 17000 Product Report Accession Number: 2021046-000
Epilog Laser Corp. is recalling Fusion Pro 24, Model 17000 due to a. A small number of Fusion Pro 24 units were released with an incorrectly placed Interlock device. As a result, the system can be operated with the f. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
a. A small number of Fusion Pro 24 units were released with an incorrectly placed Interlock device. As a result, the system can be operated with the front-loading door in an open position. b. Fails to comply with Class 2 designation, indicated in Part 6 of Laser Product Report. An incorrectly placed Interlock device can allow Class 4 laser radiation fields during operation.
Recommended Action
Per FDA guidance
The measures to be taken to repair such defect or to bring the product into compliance with the Federal standard. This Recall provides corrections by repair to a defective safety interlock location by a kit with comprehensive instructions, offered at no cost to purchasers
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