{
  "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": "2026-07-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Bentonville",
      "state": "AR",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "90359",
      "recalling_firm": "Walmart Inc",
      "address_1": "702 Sw 8th St Ms 275",
      "address_2": "",
      "postal_code": "72716-6299",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide in the USA.",
      "recall_number": "D-1159-2022",
      "product_description": "Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL, a) 100-count bottles labeled with UPC 7 501031 111190 and UPC 6 09002 40885, and b) 2 pack of 100-count bottles per carton UPC 3 72426 01434",
      "product_quantity": "1308 bottles total",
      "reason_for_recall": "Marketed Without An Unapproved NDA/ANDA: All lots were found to be unapproved drugs based on labeling claims.",
      "recall_initiation_date": "20220524",
      "center_classification_date": "20220624",
      "report_date": "20220622",
      "code_info": "All product lots.",
      "more_code_info": ""
    }
  ]
}