PlainRecalls
FDA Devices Moderate Class II Ongoing

OMTech Desktop Laser Engraver

Reported: June 19, 2024 Initiated: June 7, 2024 #Z-2129-2024

Product Description

OMTech Desktop Laser Engraver

Reason for Recall

Lack of redundant interlocks, missing required labels and certification labels as required by 21 1010.2.

Details

Units Affected
641
Distribution
US Nationwide
Location
Anaheim, CA

Frequently Asked Questions

What product was recalled?
OMTech Desktop Laser Engraver. Recalled by Rygel Advanced Machines d/b/a Omtech Laser. Units affected: 641.
Why was this product recalled?
Lack of redundant interlocks, missing required labels and certification labels as required by 21 1010.2.
Which agency issued this recall?
This recall was issued by the FDA Devices on June 19, 2024. Severity: Moderate. Recall number: Z-2129-2024.