Jinan, China
Jinan Bodor Cnc Machine Co Ltd recalls
2 recalls recorded since 2018, most recently on 7 February 2025. 2 are listed as ongoing. Status and classification are as published by the FDA.
Recalls2
Ongoing (FDA)2
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 7 February 2025
- Reason
- 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
- Initiated
- FDA Mandated
- Recall number
- Z-2149-2025
- Bodor's I series laser cutting machine.
Ongoing Class II Medical devices
- Recall started
- 19 December 2024
- Reason
- Non-compliant laser products
- Distribution
- US Nationwide Distribution
- Initiated
- FDA Mandated
- Recall number
- Z-0768-2025
- Bodor P and C series laser cutting machines
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.