# FDA recall Z-0092-2025

> **Maquet Cardiovascular, LLC** · Class I · device recall initiated 2024-09-20.

## Product

VasoView HemoPro Endoscopic Vessel Harvesting System, Product Codes VH-3000-W and VH-3500

## Reason for recall

There were reports of the silicone detaching from the Jaws of the Harvesting Tool during use.

## Distribution

Worldwide distribution. US Nationwide. Brazil, China, and Hong Kong.

## Key facts

- **Recall number:** Z-0092-2025
- **Recalling firm:** Maquet Cardiovascular, LLC
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-09-20
- **Report date:** 2024-11-06

- **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-0092-2025

## Citation

> AI Analytics. FDA recall Z-0092-2025. Retrieved 2026-09-22 from https://api.ai-analytics.org/recall/Z-0092-2025. Source: US FDA. Licensed CC0.

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