Device recall
Z-2190-2010: Spectranetics Corporation, QuickCat Extraction Catheter, REF 60090-01, Sterile…
FDA device recall · Class II · Spectranetics Corporation
Key facts
| Recall number (Z-number) | Z-2190-2010 |
|---|---|
| Recall event | 56115 |
| Product | Spectranetics Corporation, QuickCat Extraction Catheter, REF 60090-01, Sterile R, Working Length 145cm, for embolus and thrombus removal from arterial vessels. |
| Product code | DXE |
| Recalling firm | Spectranetics Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 20, 2010 |
| 510(k) numbers | K060092, K073519 |
| FEI number | 3007284006 |
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