{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Atlanta",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93475",
      "recalling_firm": "Vero Biotech, LLC",
      "address_1": "387 Technology Cir Nw Ste 125",
      "address_2": "N/A",
      "postal_code": "30313-2411",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US:  AZ and FL",
      "recall_number": "Z-0564-2024",
      "product_description": "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",
      "product_quantity": "2 cassettes",
      "reason_for_recall": "Cassette did not meet an 1n-process flow criterion.",
      "recall_initiation_date": "20231117",
      "center_classification_date": "20231215",
      "report_date": "20231227",
      "code_info": "Lot Code: W-0001-2023, Cassette serial numbers:  GA01T707, GA01T108"
    }
  ]
}