Flux Technology Inc.: Medical Device Recall in 2025 - (Recall #: Z-1878-2025)

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:

Lazervida 10W diode laser cutter and engraver with Lazervida shield.

Product Classification:

Class II

Date Initiated: February 19, 2025

Date Posted: June 11, 2025

Recall Number: Z-1878-2025

Event ID: 96935

Reason for Recall:

Lazervida 10W Diode Laser Engraver does not fully meet current Federal performance standards in certain areas. Specifically, the product does not incorporate the additional beam attenuator, remote interlock connector, key switch, specific labels and manual instructions required under current regulations.

Status: Ongoing

Product Quantity: 91

Code Information:

None.

Distribution Pattern:

Voluntary or Mandated:

FDA Mandated