Reported Dec 11, 2024 · Ongoing
Fusion Pro 24, Model 17000
Epilog Laser Corp.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Epilog Laser Corp. · 16371 Table Mountain Pkwy · Golden, CO · 80403-1826
Is this the product you have?
Fusion Pro 24Model 17000
- Lot codes and dates
- Model 17000
- Product Report Accession Number2021046-000
- Amount recalled
- 751
Where it was sold
- Nationwide
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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