Device recall
Z-0614-2011: Heartstring II Proximal Seal / VASOVIEW 6 Endoscopic Vessel Harvesting System…
FDA device recall · Class II · CTS, Inc. dba Guidant Cardiac Surgery
Key facts
| Recall number (Z-number) | Z-0614-2011 |
|---|---|
| Recall event | 51242 |
| Product | Heartstring II Proximal Seal / VASOVIEW 6 Endoscopic Vessel Harvesting System, Model Number: VH-2000, Product is manufactured and distributed by Maquet Corporation San Jose, CA |
| Product code | GCJ |
| Recalling firm | CTS, Inc. dba Guidant Cardiac Surgery |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 19, 2011 |
| 510(k) numbers | K030512 |
| 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