Jinan Bodor Cnc Machine Co Ltd: Medical Device Recall in 2025 - (Recall #: Z-2149-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

Bodor's I series laser cutting machine.

Product Classification:

Class II

Date Initiated: February 7, 2025

Date Posted: July 30, 2025

Recall Number: Z-2149-2025

Event ID: 97284

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).

Status: Ongoing

Product Quantity: 20

Code Information:

The Accession Number is 2421628- 001.

Distribution Pattern:

Voluntary or Mandated:

FDA Mandated