{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "North Chicago",
      "address_1": "1 N Waukegan Rd",
      "reason_for_recall": "",
      "address_2": "",
      "product_quantity": "673 kits",
      "code_info": "Material/List number: 629100116  Lots: 32025245, 32054247, 32265215, 32335206, 32335336",
      "center_classification_date": "20170531",
      "distribution_pattern": "Nationwide, Albania, Austria, Australia, Belgium, Bulgaria, Canada, Switzerland, Czech Republic, Germany, Denmark, Estonia, Spain, Finland, France, Great Britain, Greece, Croatia, Hungary, Ireland, Italy, Japan, Korea, Luxembourg, Netherlands, Norway, Portugal, Romania, Russia, Saudi Arabia, Sweden, Slovenia, Slovakia, Turkey",
      "state": "IL",
      "product_description": "AbbVie PEG, PEG Kit 20FR, FOR ENTERAL USE ONLY, STERILE, Rx Only.",
      "report_date": "20170607",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "AbbVie Inc.",
      "recall_number": "Z-2176-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "77129",
      "termination_date": "20190709",
      "more_code_info": "",
      "recall_initiation_date": "20170427",
      "postal_code": "60064-1802",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}