# FDA recall Z-0210-2024

> **Maquet Cardiovascular, LLC** · Class II · device recall initiated 2023-09-19.

## Product

Vasoview 6 Pro (VV6) - Endoscopic Vessel Harvesting System, Model VH-2400 printed on outer label, inner label and IFU, outer box artwork for Vasoview Hemopro 2 (HP2).

## Reason for recall

Device packaged inside an incorrect outer box; displaying artwork & illustrations for a different device.

## Distribution

US (AL, AR, CA, FL, GA, IN, KY, MI, NJ, OK, PA, TN, TX) and Canada.

## Key facts

- **Recall number:** Z-0210-2024
- **Recalling firm:** Maquet Cardiovascular, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-09-19
- **Report date:** 2023-11-08

- **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-0210-2024

## Citation

> AI Analytics. FDA recall Z-0210-2024. Retrieved 2026-09-04 from https://api.ai-analytics.org/recall/Z-0210-2024. Source: US FDA. Licensed CC0.

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