{
  "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": [
    {
      "status": "Terminated",
      "city": "Tulsa",
      "state": "OK",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "62924",
      "recalling_firm": "Physicians Total Care, Inc.",
      "address_1": "12515 E 55th St Ste 100",
      "address_2": "N/A",
      "postal_code": "74146-6234",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "FAX",
      "distribution_pattern": "VA",
      "recall_number": "D-090-2013",
      "product_description": "Enjuvia (synthetic conjugated estrogens, B) tablets, 0.3mg, 30-count tablets per bottle, Rx only, Mfg. By: Duramed Pharmaceuticals, Pomona NY 10970; Repacked & distributed by: Physicians Total Care, Inc., Tulsa, OK  74146; NDC 54868-6164-1.",
      "product_quantity": "5 bottles",
      "reason_for_recall": "Subpotent (Single ingredient) drug : This is a sub recall of Teva's Enjuvia due to low Out of Specification (OOS) assay results.",
      "recall_initiation_date": "20110408",
      "center_classification_date": "20121211",
      "termination_date": "20130222",
      "report_date": "20121219",
      "code_info": "62QJ, Exp 12/11"
    }
  ]
}