Rygel Advanced Machines d/b/a Omtech Laser: Device Recall
Recall #Z-2129-2024 · 06/07/2024
Class II: Risk
Recall Details
- Recall Number
- Z-2129-2024
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Rygel Advanced Machines d/b/a Omtech Laser
- Status
- Ongoing
- Date Initiated
- 06/07/2024
- Location
- Anaheim, CA, United States
- Voluntary/Mandated
- FDA Mandated
- Product Quantity
- 641
Reason for Recall
Lack of redundant interlocks, missing required labels and certification labels as required by 21 1010.2.
Product Description
OMTech Desktop Laser Engraver
Distribution Pattern
US Nationwide
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.