FDA recall Z-2149-2025
Jinan Bodor Cnc Machine Co Ltd · Class II · device
Product
Bodor's I series laser cutting machine.
Reason for recall
The Bodor i Series products fail to meet certain applicable Federal standards, 21 CFR 1040.10(f)(1) and 21 CFR 1040.10(f)(2).
Distribution
US
Key facts
- Status
- Ongoing
- Initiation date
- 2025-02-07
- Report date
- 2025-07-30
- Voluntary/Mandated
- FDA Mandated
- Location
- Jinan, N/A, China
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2149-2025