Bodor P and C series laser cutting machines — Class II medical device recall Z-0768-2025
Ongoing recall by Jinan Bodor Cnc Machine Co Ltd, reported 2025-01-29, distributed nationwide. Non-compliant laser products
| Recall number | Z-0768-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | FDA mandated |
| Recalling firm | Jinan Bodor Cnc Machine Co Ltd, Jinan, China |
| Recall initiated | 2024-12-19 |
| Classified | 2025-01-18 |
| Reported by FDA | 2025-01-29 |
| Distributed | Nationwide (US) |
| Quantity | 269 units |
Product
Bodor P and C series laser cutting machines
Reason for recall
Non-compliant laser products
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0768-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.