Device recall
Z-1308-06: Boston Scientific Vesica Sling Kits with Drill-In Anchor System sterile, for…
FDA device recall · Class II · Boston Scientific Corp
Key facts
| Recall number (Z-number) | Z-1308-06 |
|---|---|
| Recall event | 35724 |
| Product | Boston Scientific Vesica Sling Kits with Drill-In Anchor System sterile, for single use only; Ref/Catalog No. 820-100, UPN Product No. (M0068201000). |
| Product code | JDR |
| Recalling firm | Boston Scientific Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 17, 2007 |
| 510(k) numbers | K932925 |
| FEI number | 1828132 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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