OMTech Desktop Laser Engraver — FDA record Z-2129-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jun 7, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
OMTech Desktop Laser Engraver
Reason
Lack of redundant interlocks, missing required labels and certification labels as required by 21 1010.2.
Classification
Class II
Recalling firm
Rygel Advanced Machines d/b/a Omtech Laser
Quantity
641
Agency-reported status
Ongoing
Source record identifier
Z-2129-2024

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityModel: DF0812-40BG, USB-032B-U1

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

US Nationwide

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Jun 19, 2024
Recall initiation date
Jun 7, 2024
Center classification date
Jun 13, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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