{
  "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": "Alpharetta",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84021",
      "recalling_firm": "Avanos Medical, Inc.",
      "address_1": "5405 Windward Pkwy",
      "address_2": "N/A",
      "postal_code": "30004-3894",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution to CT, IN, MD, NJ, PA, VA.      International distribution to Great Britain.",
      "recall_number": "Z-0371-2020",
      "product_description": "CORFLO* Percutaneous Endoscopic Gastrostomy (PEG) Kit, Labeled as CORFLO* PEG Kit with ENFit Connector.  2 units per case    The devices could be branded as Halyard Health.",
      "product_quantity": "104 cases (208 units) total",
      "reason_for_recall": "The connector piece to the PEG tube does not pass over the guidewire.",
      "recall_initiation_date": "20191008",
      "center_classification_date": "20191114",
      "termination_date": "20220316",
      "report_date": "20191120",
      "code_info": "Catalog Number: 50-4016E1 (Lot Numbers:0203137961, 0203172166);      Catalog Number: 50-4020E1 (Lot Number: 0203069043)"
    }
  ]
}