Device recall
Z-1103-04: Boston Scientific/Microvasive brand Biliary Stent Kit, 7 FR x 10 cm, sterile…
FDA device recall · Class III · Boston Scientific Corp
Key facts
| Recall number (Z-number) | Z-1103-04 |
|---|---|
| Recall event | 29418 |
| Product | Boston Scientific/Microvasive brand Biliary Stent Kit, 7 FR x 10 cm, sterile, single use only; Ref 3102. |
| Product code | FGE |
| Recalling firm | Boston Scientific Corp |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 14, 2004 |
| 510(k) numbers | K834468 |
| FEI number | 1828132 |
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