# FDA recall Z-0564-2024

> **Vero Biotech, LLC** · Class II · device recall initiated 2023-11-17.

## Product

VERO BIOTECH GENOSYL DS (Delivery System) Generation 3 Cassette, Model Number 602722-01; generates and delivers nitric oxide (NO) for inhalation at the point of use

## Reason for recall

Cassette did not meet an 1n-process flow criterion.

## Distribution

US:  AZ and FL

## Key facts

- **Recall number:** Z-0564-2024
- **Recalling firm:** Vero Biotech, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-11-17
- **Report date:** 2023-12-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Atlanta, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0564-2024

## Citation

> AI Analytics. FDA recall Z-0564-2024. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0564-2024. Source: US FDA. Licensed CC0.

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