Device recall
Z-2105-2019: YXLON Cheetah cabinet X-Ray System Product Usage: The products are generally…
FDA device recall · Class II · Comet Technologies Usa Inc
Key facts
| Recall number (Z-number) | Z-2105-2019 |
|---|---|
| Recall event | 83295 |
| Product | YXLON Cheetah cabinet X-Ray System Product Usage: The products are generally used for non-destructive testing and quality control |
| Product code | RCE |
| Recalling firm | Comet Technologies Usa Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 13, 2024 |
| FEI number | 3010948215 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database