Device recall
Z-0041-2014: Xoran MiniCAT CT Scanner ID ENT00001
FDA device recall · Class II · Xoran Technologies, Inc.
Key facts
| Recall number (Z-number) | Z-0041-2014 |
|---|---|
| Recall event | 66344 |
| Product | Xoran MiniCAT CT Scanner ID ENT00001 |
| Product code | JAK |
| Recalling firm | Xoran Technologies, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 11, 2014 |
| FEI number | 3004198450 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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