Device recall
Z-0769-06: Storz Documentation Cart with Articulating Arm, Model Number 9601F
FDA device recall · Class II · Karl Storz Endoscopy America Inc
Key facts
| Recall number (Z-number) | Z-0769-06 |
|---|---|
| Recall event | 35048 |
| Product | Storz Documentation Cart with Articulating Arm, Model Number 9601F |
| Product code | KOG |
| Recalling firm | Karl Storz Endoscopy America Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 7, 2008 |
| FEI number | 2020550 |
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