Comet Technologies Usa Inc: Medical Device Recall in 2019 - (Recall #: Z-2106-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: October 1, 2018

Date Posted: August 14, 2019

Recall Number: Z-2106-2019

Event ID: 83295

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.

Status: Terminated

Product Quantity: 93

Code Information:

X-Ray Systems

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

FDA Mandated