Fusion Pro 24, Model 17000
Class I - DangerousWhat Should You Do?
- Check if you have this product: Model 17000 Product Report Accession Number: 2021046-000
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Epilog Laser Corp.
- Reason for Recall:
- 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.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
Fusion Pro 24, Model 17000
Product Codes/Lot Numbers:
Model 17000 Product Report Accession Number: 2021046-000
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0524-2025