FDA Device recall Z-2149-2025
Bodor's I series laser cutting machine
- FDA Device
- Class II
- ongoing
- Published 2025-07-30
On 2025-07-30 the FDA classified a Class II recall of Bodor's I series laser cutting machine by Jinan Bodor Cnc Machine, citing 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).
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2149-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-02-07 |
| Published | 2025-07-30 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Jinan Bodor Cnc Machine |
| Distribution | n/a |
Product
Bodor's I series laser cutting machine.
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).
Identifiers
| code_info | The Accession Number is 2421628- 001. |
|---|
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-2149-2025%22
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