Device recall
Z-2176-2024: The VASOVIEW HemoPro Endoscopic Vessel Harvesting Systems are designed for use…
FDA device recall · Class II · Maquet Cardiovascular, LLC
Key facts
| Recall number (Z-number) | Z-2176-2024 |
|---|---|
| Recall event | 94700 |
| Product | The VASOVIEW HemoPro Endoscopic Vessel Harvesting Systems are designed for use in conjunction with the 7 mm Extended Length Endoscope. The Harvesting Cannula has four lumens which house the Endoscope, C-Ring, distal lens washer tube, and harvesting tool for cutting and cauterizing vessel branches… |
| Product code | GEI |
| Recalling firm | Maquet Cardiovascular, LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K153194 |
| 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