Device recall
Z-0712-2025: Vasoview Hemopro 2 (w/Vasoshield) Endoscopic Vessel Harvesting System. Model…
FDA device recall · Class I · Maquet Cardiovascular, LLC
Key facts
| Recall number (Z-number) | Z-0712-2025 |
|---|---|
| Recall event | 95908 |
| Product | Vasoview Hemopro 2 (w/Vasoshield) Endoscopic Vessel Harvesting System. Model Numbers: VH-4001. Indicated for use in minimally invasive surgery allowing access for vessel harvesting. |
| Product code | GEI |
| Recalling firm | Maquet Cardiovascular, LLC |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K101274 |
| FEI number | 2242352 |
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