Device recall
Z-0666-2007: superDimension Bronchus System (AAS00016-01), an image-guided localization…
FDA device recall · Class II · SuperDimension, Inc.
Key facts
| Recall number (Z-number) | Z-0666-2007 |
|---|---|
| Recall event | 36947 |
| Product | superDimension Bronchus System (AAS00016-01), an image-guided localization system used to guide endoscopic tools to predetermined targets within the pulmonary tract. |
| Product code | JAK |
| Recalling firm | SuperDimension, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 20, 2008 |
| 510(k) numbers | K042438, K052260, K052852, K062315 |
| FEI number | 3004962788 |
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