VERO BIOTECH GENOSYL DS — Class II medical device recall Z-0564-2024
Ongoing recall by Vero Biotech, LLC, reported 2023-12-27, distributed in AZ, FL. Cassette did not meet an 1n-process flow criterion.
| Recall number | Z-0564-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Vero Biotech, LLC, Atlanta, GA, United States |
| Recall initiated | 2023-11-17 |
| Classified | 2023-12-15 |
| Reported by FDA | 2023-12-27 |
| Distributed | AZ, FL |
| Quantity | 2 cassettes |
| Lot numbers | W-0001-2023 |
| Serial numbers | GA01T108, GA01T707 |
| Model numbers | 602722-01 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0564-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.