FDA recall notice
Endoscopic Vessel Harvesting (EVH) System Correction: Getinge and Maquet Cardiovascular…
FDA Recall Confirmed · Endoscopic Vessel Harvesting (EVH) System · posted Jul 15, 2025
Key facts
| Notice | Endoscopic Vessel Harvesting (EVH) System Correction: Getinge and Maquet Cardiovascular Update Use Instructions for VasoView HemoPro 2 (VH-4000 and VH-4001) EVH Systems due to Risk for Bent or Detached Heater Wires and Silicone Peeling or Detaching During Use |
|---|---|
| Device type | Endoscopic Vessel Harvesting (EVH) System |
| Status | Recall Confirmed |
| Posted | Jul 15, 2025 |
| Notice on fda.gov | fda.gov |
At a glance
- Confirmed Recall confirmed
- Yes Currently listed by the FDA
- None Recall events referenced
- 1–9 UDI device identifiers named
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recall notices and early alerts
The FDA's Medical Device Recalls and Early Alerts list covers the most serious device recalls, plus early alerts about potentially high-risk device issues while the FDA is still collecting information. A notice is updated as the recall is confirmed or changes.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls and Early Alerts · Source date: