Device recall
Z-0826-2008: Xoran MiniCAT System for ENT (server and work station), Xoran Technologies, Ann…
FDA device recall · Class III · Xoran Technologies, Inc.
Key facts
| Recall number (Z-number) | Z-0826-2008 |
|---|---|
| Recall event | 45532 |
| Product | Xoran MiniCAT System for ENT (server and work station), Xoran Technologies, Ann Arbor, MI |
| Product code | JAK |
| Recalling firm | Xoran Technologies, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Oct 22, 2010 |
| 510(k) numbers | K032243 |
| FEI number | 3004198450 |
At a glance
- 1–9 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