{
  "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,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Corona",
      "address_1": "311 Bonnie Cir",
      "reason_for_recall": "Impurities/Degradation Products: Out-of-specification results were obtained for a known  impurities.",
      "address_2": "",
      "product_quantity": "63,627 cartons",
      "code_info": "432127A Exp. 01/13, 478076A Exp. 05/13, 515539B Exp.09/13",
      "center_classification_date": "20121218",
      "distribution_pattern": "Nationwide",
      "state": "CA",
      "product_description": "Caziant (desogestrel and ethinyl estradiol) Tablets, USP, (Triphasic Regimen), 0.1 mg/0.025 mg, 0.125 mg/0.025 mg, 0.15 mg/0.025 mg, 28-count tablets per dispenser (NDC 52544-959-28), packaged in 3-count Tablet Dispensers per carton (NDC 52544-959-31), Rx only Manufactured by: Watson Laboratories, Inc., Corona, CA 92880; Distributed by: Watson Pharma, Inc., Corona, CA 92880.",
      "report_date": "20121226",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Watson Laboratories Inc",
      "recall_number": "D-094-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "63906",
      "termination_date": "20131204",
      "more_code_info": "",
      "recall_initiation_date": "20121213",
      "postal_code": "92880-2882",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}