---
title: "VERO BIOTECH GENOSYL DS (Delivery System) Generation 3 Cassette, Model Number... — FDA record Z-0564-2024 | Is It on Recall"
description: "Cassette did not meet an 1n-process flow criterion."
url: https://isitonrecall.com/recall/fda-device-z-0564-2024-vero-biotech-genosyl-ds-delivery-system-generation-3-cassette-model-number-602722-01-generates-and-d/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# VERO BIOTECH GENOSYL DS (Delivery System) Generation 3 Cassette, Model Number 602722-01; generates and delivers nitri... — FDA record Z-0564-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Nov 17, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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**: Cassette did not meet an 1n-process flow criterion.
- **Classification**: Class II
- **Recalling firm**: Vero Biotech, LLC
- **Quantity**: 2 cassettes
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0564-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0564-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Lot Code: W-0001-2023, Cassette serial numbers: GA01T707, GA01T108 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US: AZ and FL

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Arizona](https://isitonrecall.com/state/arizona/)
- [Florida](https://isitonrecall.com/state/florida/)

## Dates in the source

- **Report date**: Dec 27, 2023
- **Recall initiation date**: Nov 17, 2023
- **Center classification date**: Dec 15, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0564-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Vero Biotech, LLC records](https://isitonrecall.com/brand/vero-biotech-llc/)