Device recall
Z-0434-05: VISTA BRITE TIP RDC(1) Guiding Catheter. Product Code 67021055, lot X0704002…
FDA device recall · Class III · Cordis Corporation
Key facts
| Recall number (Z-number) | Z-0434-05 |
|---|---|
| Recall event | 30637 |
| Product | VISTA BRITE TIP RDC(1) Guiding Catheter. Product Code 67021055, lot X0704002, Precutaneous Catheter. |
| Product code | DQY |
| Recalling firm | Cordis Corporation |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 19, 2008 |
| 510(k) numbers | K021593 |
| FEI number | 1016427 |
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