{
  "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": "89132",
      "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": "E-Mail",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the states of Oklahoma and Ohio; The countries of China, France, Germany, Great Britain, Greece, Italy, and Netherlands.",
      "recall_number": "Z-0847-2022",
      "product_description": "BALLARD* Multi-Access Port (MAP) Catheter, Double Swivel Y- Adult, 16 French; Sterile; Single Use",
      "product_quantity": "2,520 devices (126 cases)",
      "reason_for_recall": "Product was distributed with incorrect expiration date.",
      "recall_initiation_date": "20211122",
      "center_classification_date": "20220331",
      "termination_date": "20230131",
      "report_date": "20220406",
      "code_info": "Finished Product Code: 102007202; Alternate Code: 240168-5; Lot No.: 30135997, 30137462, 30138710, 30140310, and 30141359."
    }
  ]
}