{
  "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": "2026-09-09",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 4
    }
  },
  "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-1158-2022",
      "product_description": "Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets, ORIGINAL, 100-count bottles, UPC 7 501031 12705.",
      "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": ""
    }
  ]
}