Device recall
Z-0259-2008: Boston Scientific 6F Guider Softip XF Guiding Catheter, 6 French, 40 degree…
FDA device recall · Class III · Boston Scientific Target
Key facts
| Recall number (Z-number) | Z-0259-2008 |
|---|---|
| Recall event | 38445 |
| Product | Boston Scientific 6F Guider Softip XF Guiding Catheter, 6 French, 40 degree angle, 90cm usable length, Material Number (UPN) H965100420, Catalog Number : 10042, Made in USA: 5905 Nathan Lane, Plymouth, MN 55442 USA |
| Product code | DQY |
| Recalling firm | Boston Scientific Target |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 5, 2007 |
| 510(k) numbers | K980453 |
| FEI number | 2939204 |
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