FDA Device recall Z-2129-2024
OMTech Desktop Laser Engraver
- FDA Device
- Class II
- ongoing
- Published 2024-06-19
On 2024-06-19 the FDA classified a Class II recall of OMTech Desktop Laser Engraver by Rygel Advanced Machines, citing lack of redundant interlocks, missing required labels and certification labels as required by 21 1010.2.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2129-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-06-07 |
| Published | 2024-06-19 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Rygel Advanced Machines |
| Distribution | US |
Product
OMTech Desktop Laser Engraver
Reason
Lack of redundant interlocks, missing required labels and certification labels as required by 21 1010.2.
Identifiers
| code_info | Model: DF0812-40BG, USB-032B-U1 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2129-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.