---
title: "Bodor's I series laser cutting machine. — FDA record Z-2149-2025 | Is It on Recall"
description: "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)."
url: https://isitonrecall.com/recall/fda-device-z-2149-2025-bodor-s-i-series-laser-cutting-machine/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Bodor's I series laser cutting machine. — FDA record Z-2149-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Feb 7, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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).
- **Classification**: Class II
- **Recalling firm**: Jinan Bodor Cnc Machine Co Ltd
- **Quantity**: 20
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2149-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2149-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | The Accession Number is 2421628- 001. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Jul 30, 2025
- **Recall initiation date**: Feb 7, 2025
- **Center classification date**: Jul 23, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2149-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Jinan Bodor Cnc Machine Co Ltd records](https://isitonrecall.com/brand/jinan-bodor-cnc-machine-co-ltd/)