# FDA recall Z-2106-2019

> **Comet Technologies Usa Inc** · Class II · device recall initiated 2018-10-01.

## Product

YXLON Cougar Cabinet X-Ray System    Product Usage:  The products are generally used for non-destructive testing and quality control

## Reason for recall

Failure to meet the requirement of the performance standard for cabinet x-ray systems (21 CFR 1020.40) for a door interlock that causes physical disconnection of the power supply using only the movement of the door.

## Distribution

US Nationwide Distribution

## Key facts

- **Recall number:** Z-2106-2019
- **Recalling firm:** Comet Technologies Usa Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-10-01
- **Report date:** 2019-08-14
- **Termination date:** 2024-06-13

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Shelton, CT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2106-2019

## Citation

> AI Analytics. FDA recall Z-2106-2019. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-2106-2019. Source: US FDA. Licensed CC0.

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