{
  "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": "Oklahoma City",
      "address_1": "3300 NW 56th Street",
      "reason_for_recall": "Non-Sterility: The recalled lot failed sterility testing.",
      "address_2": "Suite 101",
      "product_quantity": "122 Pellets",
      "code_info": "Lot # 06241401-070714Q, Exp 12/14",
      "center_classification_date": "20150504",
      "distribution_pattern": "AZ and KS",
      "state": "OK",
      "product_description": "Epel 18 mg Estradiol Pellet, For In Office Use Only, For In Office Administration Only, Not for Resale or Dispensing to an Individual Patient, Rx Only, Preferred Physician Medical LLC, 405-551-8216",
      "report_date": "20150513",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Physician Preferred Medical, LLC",
      "recall_number": "D-0982-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "70703",
      "termination_date": "20170117",
      "recall_initiation_date": "20140724",
      "postal_code": "73112",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}