Official recall record
Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3000-W .
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2023-12-01
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00607567700413
- Brand on record
- Maquet Cardiovascular, LLC
What the authority reported
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.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Record last checked against the registry on 2026-05-31.
Same barcode in other registries
The same EAN appears in 1 other official recall record(s) — a cross-border signal worth checking if you bought this product abroad.
- 2024-09-20 · US FDA — Medical Devices
VasoView HemoPro Endoscopic Vessel Harvesting System, Product Codes VH-3000-W and VH-3500
Other recalls from this brand
- 2026-06-02 · US FDA — Medical Devices
The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000; UDI 00607567700406) is a sterile, - 2025-08-06 · US FDA — Medical Devices
Vasoview Hemopro 3 Endoscopic Vessel Harvesting System Model No. C-VH-6000. The VASOVIEW HEMOPRO 3 Endoscopi - 2025-03-20 · US FDA — Medical Devices
The VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System is designed for use in conjunction with the 7 mm ex
All 9 official recall notices naming Maquet Cardiovascular, LLC on this site →