Device recall
Z-1102-06: Boston Scientific Wiseguide Guide Catheter 7F,.076 '', Femoral Approach…
FDA device recall · Class II · Boston Scientific
Key facts
| Recall number (Z-number) | Z-1102-06 |
|---|---|
| Recall event | 35515 |
| Product | Boston Scientific Wiseguide Guide Catheter 7F, .076 '', Femoral Approach, Manufactured for Boston Scientific Scimed, Inc., One Scimed Place, Maple Grove, MN USA 55311. Nonpyrogenic. |
| Product code | DQY |
| Recalling firm | Boston Scientific |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 30, 2006 |
| 510(k) numbers | K974684 |
| 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