{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Alpharetta",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98907",
      "recalling_firm": "Avanos Medical, Inc.",
      "address_1": "5405 Windward Pkwy",
      "address_2": "N/A",
      "postal_code": "30004-4667",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-2333-2026",
      "product_description": "Brand Name: CORFLO  Product Name: CORFLO* Safety PEG Kit  Model/Catalog Number: 30-4320",
      "product_quantity": "231 kits",
      "reason_for_recall": "Lidocaine hydrochloride injection, the subject of a supplier recall for  quality issues, were included into sterile kits and sets.",
      "recall_initiation_date": "20260430",
      "center_classification_date": "20260605",
      "report_date": "20260617",
      "code_info": "UDI-DI 10350770007585, Lot Numbers 30365226 and 30382750"
    }
  ]
}