FDAFDA · Food and drugs·Recall number Z-2106-2019
YXLON Cougar Cabinet X-Ray System Product Usage: The products are generally used for non-destructive testing and quality control
Published August 14, 2019 · Recall initiated: October 1, 2018
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
FDA Mandated · Letter
Recall details
- Manufacturer
- Comet Technologies Usa Inc
- Distributor
- US Nationwide Distribution
- Lot
- X-Ray Systems
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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