FDA Device recall Z-0768-2025
Bodor P and C series laser cutting machines
- FDA Device
- Class II
- ongoing
- Published 2025-01-29
On 2025-01-29 the FDA classified a Class II recall of Bodor P and C series laser cutting machines by Jinan Bodor Cnc Machine, citing non-compliant laser products.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0768-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-12-19 |
| Published | 2025-01-29 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Jinan Bodor Cnc Machine |
| Distribution | US |
Product
Bodor P and C series laser cutting machines
Reason
Non-compliant laser products
Identifiers
| code_info | P series is 2421537-000 and C series is 2421612-000. |
|---|
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-0768-2025%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.