Device recall
Z-0292-04: Guidant Brand VasoView 5 Harvesting Cannula System, Model Number: VH-1000
FDA device recall · Class II · Guidant Cardiac Surgery
Key facts
| Recall number (Z-number) | Z-0292-04 |
|---|---|
| Recall event | 27884 |
| Product | Guidant Brand VasoView 5 Harvesting Cannula System, Model Number: VH-1000 |
| Product code | HET |
| Recalling firm | Guidant Cardiac Surgery |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 9, 2004 |
| 510(k) numbers | K020143 |
| FEI number | 3000719698 |
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