Comet Technologies Usa Inc recalls YXLON Cheetah cabinet X-Ray System Product Usage: The products are generally used for non-destructive testing and quali…

Recall date

October 1, 2018

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2105-2019

FDA classification

Class II

Brand / firm

Comet Technologies Usa Inc

Sold / distributed

US Nationwide Distribution

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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