FDA Device recall Z-0723-2024
Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3000-W
- FDA Device
- Class II
- ongoing
- Published 2024-01-24
On 2024-01-24 the FDA classified a Class II recall of Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3000-W by Maquet Cardiovascular, citing risk of polyimide particulate matter being present on the endoscopic harvesting vessel system. This issue may result in polyimide particulate matter being introduced into the arte….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0723-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-12-01 |
| Published | 2024-01-24 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Maquet Cardiovascular |
| Distribution | n/a |
Product
Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3000-W .
Reason
Risk of polyimide particulate matter being present on the endoscopic harvesting vessel system. This issue may result in polyimide particulate matter being introduced into the arterial conduit for patients undergoing a coronary artery bypass graft (CABG) or peripheral bypass graft surgery.
Identifiers
| code_info | UDI-DI: 00607567700413, Lots: 3000283735, 3000293031, 3000310304, 3000333956. |
|---|
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-0723-2024%22
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