{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Atlanta",
      "state": "GA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87764",
      "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": "Distributed nationwide to TX, MD, VA, GA, FL, KS, LA, MN, and NC",
      "recall_number": "Z-1863-2021",
      "product_description": "GENOSYL DS; Nitric Oxide Delivery System    Combination Product NDA202860",
      "product_quantity": "465 units",
      "reason_for_recall": "Reports received of NO measured below desired dose during transition between primary console and backup console since Software Version 2.2.3 was uploaded to consoles in the field.",
      "recall_initiation_date": "20210519",
      "center_classification_date": "20210623",
      "termination_date": "20231012",
      "report_date": "20210630",
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}