[Recalled] YXLON Cheetah cabinet X-Ray System Product Usage: The products are generally used for non-destructive testing and quality control — Failure to meet the requirement of the performance standard for cabinet x-ray s… | FDA 2018-1
A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.
Recall details
| Product | YXLON Cheetah cabinet X-Ray System Product Usage: The products are generally used for non-destructive testing and quality control |
|---|---|
| Brand / manufacturer | Comet Technologies Usa Inc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2105-2019 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 01 October 2018 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: 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.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Comet Technologies Usa Inc
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.