FDA Device recall Z-0711-2025
VasoView HemoPro 2 Endoscopic Vessel Harvesting System
- FDA Device
- Class I
- ongoing
- Published 2025-01-15
On 2025-01-15 the FDA classified a Class I recall of VasoView HemoPro 2 Endoscopic Vessel Harvesting System by Maquet Cardiovascular, citing potential for two issues: 1. Bent or detached heater wire; 2. Silicone peeling or detaching from the Jaws of the Harvesting Tool.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0711-2025 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2024-12-09 |
| Published | 2025-01-15 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Maquet Cardiovascular |
| Distribution | US |
Product
VasoView HemoPro 2 Endoscopic Vessel Harvesting System. Model Numbers: VH-4000. Indicated for use in minimally invasive surgery allowing access for vessel harvesting.
Reason
Potential for two issues: 1. Bent or detached heater wire; 2. Silicone peeling or detaching from the Jaws of the Harvesting Tool
Identifiers
| code_info | Model Number: VH-4000. UDI-DI: 00607567700406. All unexpired Lots. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0711-2025%22
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