Device recall
Z-0454-05: RunWay 6F Cardiovascular Guide Catheter.
FDA device recall · Class II · Boston Scientific Scimed
Key facts
| Recall number (Z-number) | Z-0454-05 |
|---|---|
| Recall event | 30405 |
| Product | RunWay 6F Cardiovascular Guide Catheter. |
| Product code | DQY |
| Recalling firm | Boston Scientific Scimed |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 10, 2006 |
| 510(k) numbers | K033441 |
| FEI number | 3002095335 |
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