{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Fajardo",
      "address_1": "Road 195, Km 1.1",
      "reason_for_recall": "Chemical contamination: Firm's inspection discovered the  presence of 2-phenylphenol in the product due to migration from the cardboard cartons in which the product is packaged.",
      "address_2": "Union Street",
      "product_quantity": "27,509 bottles",
      "code_info": "Lot# 510122B; exp 04/13",
      "center_classification_date": "20130430",
      "distribution_pattern": "US Nationwide and Puerto Rico",
      "state": "PR",
      "product_description": "Femhrt (norethindrone acetate and ethinyl estradiol) tablets,  0.5 mg/2.5 mcg, 90 count bottle (NDC#: 0430-0145-23), Rx only,  Manufactured by Warner Chilcott Company, LLC, Fajardo, PR 00738, Marketed by Warner Cholcott (US), LLC, Rockaway, NJ 07866",
      "report_date": "20130508",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Warner Chilcott Company LLC",
      "recall_number": "D-303-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "64459",
      "termination_date": "20140609",
      "more_code_info": "",
      "recall_initiation_date": "20130215",
      "postal_code": "00738",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}