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Unrated Medical device recall · FDA · Published November 17, 2023

Vero Biotech Genosyl DS Cassette Recall: Nitric Oxide Risk

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.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-0564-2024Medical deviceVero Biotech ›
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Contact the company

Recalling firmVero Biotech, LLC387 Technology Cir Nw Ste 125 · Atlanta, GA 30313-2411
✎ GovInfoNow plain-language explainer

Vero Biotech is recalling its Genosyl DS Generation 3 Cassette (Model 602722-01) because it didn't meet a manufacturing flow standard. This could lead to improper nitric oxide delivery during use, potentially causing inhalation risks. Read more at govinfonow.com/recall/56805-vero-biotech-genosyl-ds-cassette-recall-nitric-oxide-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/56805-vero-biotech-genosyl-ds-cassette-recall-nitric-oxide-risk · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0564-2024

Cite this page

“Vero Biotech Genosyl DS Cassette Recall: Nitric Oxide Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/56805-vero-biotech-genosyl-ds-cassette-recall-nitric-oxide-risk. Based on FDA recall #Z-0564-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0564-2024%22&limit=1).

Vero Biotech, LLC voluntarily recalled its VERO BIOTECH GENOSYL DS (Delivery System) Generation 3 Cassette because it did not meet an in-process flow criterion, according to the FDA on November 17, 2023.

How to tell if you have it

  • Brand: Vero Biotech
  • Product: VERO BIOTECH GENOSYL DS (Delivery System) Generation 3 Cassette
  • Model Number: 602722-01
  • Lot Code: W-0001-2023
  • Cassette serial numbers: GA01T707, GA01T108
  • Quantity: 2 cassettes
  • Distribution: AZ and FL

The hazard

The cassette did not meet an in-process flow criterion, according to the FDA.

Context

GovInfoNow's records show Vero Biotech, LLC has 2 other recalls on record since 2021-05-19. Other recent recalls of similar products include NOXBOX Nitric Oxide Delivery System Recall (2026-08-19), Codman CerebroFlo EVD Catheter Recall (2026-04-10) and Philips Integris-Allura System Recall (2026-04-28).

How to tell if you have this one

Check for the model number 602722-01 on the cassette. The lot code W-0001-2023 and serial numbers GA01T707 or GA01T108 indicate affected units.

  • Brand
    Vero Biotech
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Verify the model number, lot code, and serial numbers to confirm if your cassette is affected.

Where it went and when

Where it was distributed

Distributed in Arizona and Florida.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: yesAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: yesFL

FDA distribution: “US: AZ and FL” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, Florida.

Recall timeline

FDA published this recall 40 days after the firm started it.

1. Firm started the recall: Nov 17, 202312. FDA classified it Class II: Dec 15, 202323. Published in FDA’s Enforcement Report: Dec 27, 202332023
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-0564-2024 (November 17, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0564-2024 to see it in context.
  • Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA