Vero Biotech, LLC recalls
Every recall we track for Vero Biotech, LLC — 3 in all, from 2021–2023 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
3 recalls since 2017.
All FDA recall records for Vero Biotech, LLC since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 1 | 0 | 1 | 0 | 2 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 1 | 1 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Vero Biotech, LLC product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Vero Biotech, LLC recalls
3 shown- UnratedMedical device
Vero Biotech, LLC recalls VERO BIOTECH GENOSYL DS (Delivery System) Generation 3 Cassette, Model Number 602722-01; generates and delivers nitric
Vero Biotech recalls Genosyl DS Generation 3 Cassette (Model 60272: W-0001-2023) due to potential nitric oxide delivery issues. Affected units may pose inhalation risks.
Vero BiotechNov 17, 2023 - Stop using nowMedical device
Vero Biotech, LLC recalls GENOSYL DS (Delivery System) console, for use as a vasodilator.
Vero Biotech recalls GENOSYL DS consoles for vasodilator use due to manufacturing defect causing nitrogen dioxide instead of nitric oxide delivery. Affected units have specific model and serial numbers.
Vero BiotechSep 9, 2021 - Lower riskMedical device
Vero Biotech, LLC recalls GENOSYL DS; Nitric Oxide Delivery System Combination Product NDA202860
Vero Biotech recalls GENOSYL DS nitric oxide delivery system with serial numbers listed; reports of insufficient nitric oxide delivery during console transitions after software update 2.2.3.
Vero BiotechMay 19, 2021
Vero Biotech, LLC recall questions
How many recalls has Vero Biotech, LLC had?
3 recalls from Vero Biotech, LLC are on record with U.S. safety agencies, from 2021–2023.
What is the most recent Vero Biotech, LLC recall?
Vero Biotech, LLC recalls VERO BIOTECH GENOSYL DS (Delivery System) Generation 3 Cassette, Model Number 602722-01; generates and delivers nitric, dated Nov 17, 2023. Every Vero Biotech, LLC recall is listed on this page, newest first.
What should I do if I have a recalled Vero Biotech, LLC product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Vero Biotech, LLC recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.