Device recall
Z-1487-04: Alveolus Tracheobronchial Stent Technology System (TB-STS), Manufactured for…
FDA device recall · Class II · Alveolus, Inc.
Key facts
| Recall number (Z-number) | Z-1487-04 |
|---|---|
| Recall event | 29886 |
| Product | Alveolus Tracheobronchial Stent Technology System (TB-STS), Manufactured for: Alveolus Inc., 401 North Tryon Street, Charlotte, North Carolina USA 28202 |
| Product code | FWN |
| Recalling firm | Alveolus, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 12, 2005 |
| 510(k) numbers | K040523 |
| FEI number | 3004039296 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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