{
  "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": "North Wales",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "78590",
      "recalling_firm": "Teva Pharmaceuticals USA",
      "address_1": "1090 Horsham Rd",
      "address_2": "",
      "postal_code": "19454-1505",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the USA and Puerto Rico",
      "recall_number": "D-0125-2018",
      "product_description": "Amethyst (Levonorgestrel and Ethinyl Estradiol Tablets USP, 90mcg/20mcg),  28 tablet dispenser (blister foil unit), Rx only, Manufactured by: Warner Chilcott Company, LLC Fajardo, Puerto Rico 00738: Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054 USA, NDC-52544-295-28",
      "product_quantity": "5,374 blister cards/28 tablets",
      "reason_for_recall": "Labeling: Incorrect Instructions. \"TABLETS IN WEEK 4 ARE INACTIVE\"  printed on the blister foil and package insert, however,all tablets are active.",
      "recall_initiation_date": "20171120",
      "center_classification_date": "20171220",
      "termination_date": "20180621",
      "report_date": "20171227",
      "code_info": "Lot # 544637A",
      "more_code_info": ""
    }
  ]
}