{
  "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": "Chicago",
      "state": "IL",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "61818",
      "recalling_firm": "Morton Salt Co.",
      "address_1": "123 N Wacker Dr",
      "address_2": "N/A",
      "postal_code": "60606-1743",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide & PR & Ireland.",
      "recall_number": "D-1656-2012",
      "product_description": "Morton, Sodium Chloride, USP, Granular, packaged in kraft paper bags, fiber drums, and semi-bulk bags.  Product is shipped in 80 lb bags, 350 lb drums & 2000 lb semi-bulk sacks.  Manufactured by Morton Salt, Inc., Chicago, Illinois 60606-1743.",
      "product_quantity": "531,950 lbs",
      "reason_for_recall": "Impurities/Degradation Products: The product was found to contain a slightly out of specification level of bromides, exceeding the bromides limit for USP Sodium Chloride.",
      "recall_initiation_date": "20120508",
      "center_classification_date": "20120820",
      "termination_date": "20130301",
      "report_date": "20120829",
      "code_info": "Lot #: OCT251BC01, NOV041BA01 & NOV071BA01."
    }
  ]
}