Device recall
Z-1106-04: Boston Scientific brand Nephroureteral Stent System. Contents: 1-8Fr percuflex…
FDA device recall · Class III · Boston Scientific Corp
Key facts
| Recall number (Z-number) | Z-1106-04 |
|---|---|
| Recall event | 29486 |
| Product | Boston Scientific brand Nephroureteral Stent System. Contents: 1-8Fr percuflex catheter with stent and locking pigtail, 1-stiffening cannula and 1-luer cap with septum. REF/catalog no. 90-6885; model no. M001906885. |
| Product code | GBO |
| Recalling firm | Boston Scientific Corp |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 23, 2004 |
| 510(k) numbers | K820867 |
| FEI number | 1828132 |
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