Device recall
Z-2039-2014: Essential NEO, Audio/Visual Integration Unit An audio/visual integration unit.
FDA device recall · Class II · Karl Storz Endoscopy
Key facts
| Recall number (Z-number) | Z-2039-2014 |
|---|---|
| Recall event | 68646 |
| Product | Essential NEO, Audio/Visual Integration Unit An audio/visual integration unit. |
| Product code | LMD |
| Recalling firm | Karl Storz Endoscopy |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 13, 2015 |
| FEI number | 3007475226 |
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