{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Des Moines",
      "state": "IA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Food",
      "event_id": "71942",
      "recalling_firm": "Heartland Products Inc.",
      "address_1": "5016 Park Avenue",
      "address_2": "N/A",
      "postal_code": "50321",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Product was distributed in IA and IL.  No foreign, military, or federal goverment distribution.",
      "recall_number": "F-1075-2016",
      "product_description": "Dough base/premix packaged in 30-lb. poly-lined cardboard boxes, manufactured under the following labels:    (1) Heartland Products, Inc. Fancy Breads Italian Base, 090108.   Manufactured by Heartland Products, Inc., Des Moines, IA; and    (2) Northern Lights Pizza, 090108, Manufactured by Heartland Products, Inc., Des Moines, IA.",
      "product_quantity": "(1) 24 - 30 lb. boxes and (2) 24- 30 lb. boxes",
      "reason_for_recall": "Presence of high levels of Azodicarbonamide (ADA), failure to declare allergens on label, and potential cross-contamination with allergens.",
      "recall_initiation_date": "20150827",
      "center_classification_date": "20160413",
      "termination_date": "20160414",
      "report_date": "20160420",
      "code_info": "(1) G0601 and (2) G0301",
      "more_code_info": ""
    }
  ]
}