Device recall
Z-0766-2008: CORDIS "Dura Star" 3.00 x 20 Dilatation Catheter, Catalog # 70120300…
FDA device recall · Class I · Cordis Corporation
Key facts
| Recall number (Z-number) | Z-0766-2008 |
|---|---|
| Recall event | 46378 |
| Product | CORDIS "Dura Star" 3.00 x 20 Dilatation Catheter, Catalog # 70120300, Distributed by Cordis Corporation, Miami Lakes, FL 33014 |
| Product code | LOX |
| Recalling firm | Cordis Corporation |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Oct 20, 2009 |
| PMA numbers | P880003 |
| FEI number | 1016427 |
At a glance
- None Linked 510(k)s
- 10–99 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