{
  "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": "St Petersburg",
      "state": "FL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "77899",
      "recalling_firm": "International Laboratories, Inc.",
      "address_1": "2701 75th St N",
      "address_2": "N/A",
      "postal_code": "33710-2938",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.A. nationwide and Puerto Rico",
      "recall_number": "D-0102-2018",
      "product_description": "Pravastatin Sodium Tablets, USP, 40 mg, 30-count bottle, Rx only, Packaged for: International Laboratories, LLC. St. Petersburg, FL 33710, NDC 54458-925-16",
      "product_quantity": "82056 bottles",
      "reason_for_recall": "Labeling: Label mix-up, the product labeled as Pravastatin sodium tablets 40 mg was filled with Bupropion hydrochloride XL Tablets 300 mg.",
      "recall_initiation_date": "20170807",
      "center_classification_date": "20171201",
      "termination_date": "20190502",
      "report_date": "20171213",
      "code_info": "Lot # 115698A, Exp 02/19",
      "more_code_info": ""
    }
  ]
}