---
title: "Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3000-W . — FDA record Z-0723-2024 | Is It on Recall"
description: "Risk of polyimide particulate matter being present on the endoscopic harvesting vessel system. This issue may result in polyimide particulate matter being intro"
url: https://isitonrecall.com/recall/fda-device-z-0723-2024-vasoview-hemopro-endoscopic-vessel-harvesting-system-model-vh-3000-w/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3000-W . — FDA record Z-0723-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Dec 1, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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.
- **Classification**: Class II
- **Recalling firm**: Maquet Cardiovascular, LLC
- **Quantity**: 554 units (OUS)
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0723-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0723-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI-DI: 00607567700413, Lots: 3000283735, 3000293031, 3000310304, 3000333956. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US: OUS: China, Brazil, Hong Kong.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Jan 24, 2024
- **Recall initiation date**: Dec 1, 2023
- **Center classification date**: Jan 12, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0723-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Maquet Cardiovascular, LLC records](https://isitonrecall.com/brand/maquet-cardiovascular-llc/)