# FDA recall Z-0870-2020

> **Energetiq Technology Inc** · Class II · device recall initiated 2019-09-27.

## Product

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.

## 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.

## Distribution

Worldwide Distribution.

## Key facts

- **Recall number:** Z-0870-2020
- **Recalling firm:** Energetiq Technology Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2019-09-27
- **Report date:** 2020-02-05

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Woburn, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0870-2020

## Citation

> AI Analytics. FDA recall Z-0870-2020. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0870-2020. Source: US FDA. Licensed CC0.

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