# FDA recall Z-0712-2025

> **Maquet Cardiovascular, LLC** · Class I · device recall initiated 2024-12-09.

## Product

Vasoview Hemopro 2 (w/Vasoshield) Endoscopic Vessel Harvesting System. Model Numbers: VH-4001.  Indicated for use in minimally invasive surgery allowing access for vessel harvesting.

## Reason for recall

Potential for two issues:   1. Bent or detached heater wire;  2. Silicone peeling or detaching from the Jaws of the Harvesting Tool

## Distribution

Nationwide distribution.  International distribution to Australia, Austria, Bahrain, Bangladesh, Belgium, Canada, Czech Republic, Denmark, Finland, France, Germany, Guatemala, Hong Kong, India, Iran, Iraq, Ireland, Italy, Japan, Jordan, Kenya, Kuwait, Malaysia, Mexico, Netherlands, Netherlands, New Zealand, Oman, Panama, Puerto Rico, Philippines, Poland, Portugal, Qatar, Saudi Arabia, Singapore, South Africa, South Korea, Spain, Sweden, Switzerland, Turkey, United Arab Emirates.

## Key facts

- **Recall number:** Z-0712-2025
- **Recalling firm:** Maquet Cardiovascular, LLC
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-12-09
- **Report date:** 2025-01-15

- **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-0712-2025

## Citation

> AI Analytics. FDA recall Z-0712-2025. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0712-2025. Source: US FDA. Licensed CC0.

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