{
  "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": "Completed",
      "city": "Atlanta",
      "state": "GA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88558",
      "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": "Letter",
      "distribution_pattern": "Distributed within US to Texas and Illinois.",
      "recall_number": "Z-2587-2021",
      "product_description": "GENOSYL DS (Delivery System) console, for use as a vasodilator.",
      "product_quantity": "120 consoles (3 consoles affected)",
      "reason_for_recall": "Manufacturing defect involving reversal of the inlet and outlet gas lines, resulting in delivery of nitrogen dioxide (NO2) instead of nitric oxide (NO).",
      "recall_initiation_date": "20210909",
      "center_classification_date": "20210930",
      "report_date": "20211006",
      "code_info": "Model Number: 601588-01, Serial Numbers G0294 (UDI (01)00850000962026(11)200728(21)G0294); G0378 (UDI (01)00850000962026(11)200917(21)G0378); and MA000065 (UDI (01)00850000962026(11)210511(21)MA000065)"
    }
  ]
}