Recall Z-2149-2025— Jinan Bodor Cnc Machine Co Ltd
Class II · Ongoing
Class II FDA medical device recall by Jinan Bodor Cnc Machine Co Ltd, initiated 2025-02-07. FDA's recall record names no specific 510(k) clearance for this event. 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)..
- Recalling firm
- Jinan Bodor Cnc Machine Co Ltd
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2025-02-07
- Firm location
- Jinan, N/A, China
Product description
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).
Data sourced from openFDA. This site is unofficial and independent of the FDA.