{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "North Chicago",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75794",
      "recalling_firm": "AbbVie Inc.",
      "address_1": "1 N Waukegan Rd",
      "address_2": "N/A",
      "postal_code": "60064-1802",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S. consignees located throughout the country and Puerto Rico. Foreign Consignees: Worldwide.",
      "recall_number": "Z-0786-2017",
      "product_description": "AbbVie PEG Kit 20 FR",
      "product_quantity": "541 units",
      "reason_for_recall": "AbbVie is issuing an urgent field correction notification due to an increased number of reports of disconnections of the AbbVie 20FR PEG tube from the Y-connectors.",
      "recall_initiation_date": "20161122",
      "center_classification_date": "20161217",
      "termination_date": "20190709",
      "report_date": "20161228",
      "code_info": "AbbVie PEG Kit 20 Fr    Product Code 62912-01-16 with lot numbers: 32025245, 32265215, 32335206, 32335336"
    }
  ]
}