Energetiq Technology Inc: Medical Device Recall in 2020 - (Recall #: Z-0870-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

EQ-400-RH-QZ and EQ-400-LH-BK products Product Usage: The device is a very broadband light source emitting incoherent non-laser light from the Deep UV through the visible wavelengths.

Product Classification:

Class II

Date Initiated: September 27, 2019

Date Posted: February 5, 2020

Recall Number: Z-0870-2020

Event ID: 84378

Reason for Recall:

On September 27, 2019 Energetiq Technology (the manufacturer) discovered a problem with their EQ-400-RH-QZ and EQ-400-LH-BK products during routine manufacturing functional testing. It was noted that a safety interlock within the lamp does not function in a reliable manner to shut down the system if the laser collimator is removed from the lamp while the system is operating. This is a potential safety hazard for anyone working on or nearby the lamp.

Status: Ongoing

Product Quantity: 15

Code Information:

The defect concerns a total of fifteen (15) of our EQ-400 products. manufactured between June 3, 2016 and September 26, 2019.

Distribution Pattern:

Worldwide Distribution.

Voluntary or Mandated:

FDA Mandated