Device recall
Z-0476-2009: VASOVIEW 4 Endoscopic Vessel Harvesting System, with VASOVIEW Flexible…
FDA device recall · Class II · CTS, Inc. dba Guidant Cardiac Surgery
Key facts
| Recall number (Z-number) | Z-0476-2009 |
|---|---|
| Recall event | 49550 |
| Product | VASOVIEW 4 Endoscopic Vessel Harvesting System, with VASOVIEW Flexible Endoscopic Tools in the following configurations: VH-10242: Uniport plus dissection cannula, short port blunt tip trocar, flexible endoscopic scissors; and VH-10243: Uniport plus dissection cannula, short port blunt tip trocar… |
| Product code | GCJ |
| Recalling firm | CTS, Inc. dba Guidant Cardiac Surgery |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 8, 2010 |
| 510(k) numbers | K035012 |
| FEI number | 3000719698 |
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