{
  "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": "PEG kits have the potential for one of the following defects: missing components, duplicate components or missing label/Instructions for Use, which includes expiry information.",
      "address_2": "",
      "product_quantity": "3,331 kits",
      "code_info": "Material/List number: 62918001  Lots: 32044225, 32155205, 32344326, 32461215",
      "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 15FR, FOR ENTERAL USE ONLY, STERILE, Rx Only.",
      "report_date": "20170607",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "AbbVie Inc.",
      "recall_number": "Z-2178-2017",
      "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"
    }
  ]
}