# FDA recall Z-0724-2024

> **Maquet Cardiovascular, LLC** · Class II · device recall initiated 2023-12-01.

## Product

Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3500.

## Reason for recall

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.

## Distribution

US:  OUS: China, Brazil, Hong Kong.

## Key facts

- **Recall number:** Z-0724-2024
- **Recalling firm:** Maquet Cardiovascular, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-12-01
- **Report date:** 2024-01-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Wayne, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0724-2024

## Citation

> AI Analytics. FDA recall Z-0724-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0724-2024. Source: US FDA. Licensed CC0.

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