Jinan Bodor Cnc Machine Co Ltd: Medical Device Recall in 2025 - (Recall #: Z-0768-2025)

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 P and C series laser cutting machines

Product Classification:

Class II

Date Initiated: December 19, 2024

Date Posted: January 29, 2025

Recall Number: Z-0768-2025

Event ID: 96035

Reason for Recall:

Non-compliant laser products

Status: Ongoing

Product Quantity: 269 units

Code Information:

P series is 2421537-000 and C series is 2421612-000.

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

FDA Mandated