Rygel Advanced Machines d/b/a Omtech Laser: Medical Device Recall in 2024 - (Recall #: Z-2129-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

OMTech Desktop Laser Engraver

Product Classification:

Class II

Date Initiated: June 7, 2024

Date Posted: June 19, 2024

Recall Number: Z-2129-2024

Event ID: 94785

Reason for Recall:

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

Status: Ongoing

Product Quantity: 641

Code Information:

Model: DF0812-40BG, USB-032B-U1

Distribution Pattern:

US Nationwide

Voluntary or Mandated:

FDA Mandated