{
  "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": [
    {
      "status": "Terminated",
      "city": "Horsham",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "67809",
      "recalling_firm": "Teva Pharmaceuticals USA",
      "address_1": "425 Privet Rd",
      "address_2": "",
      "postal_code": "19044-1220",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "NY and KY",
      "recall_number": "D-1354-2014",
      "product_description": "ParaGard T 380A - Intrauterine Copper Contraceptive, 176 mg of copper wire, Duramed Pharmaceuticals Inc, a subsidiary of Barr Pharmaceuticals, Inc., Pomona, NY",
      "product_quantity": "47890",
      "reason_for_recall": "Non-sterility: due to a failed sterility test",
      "recall_initiation_date": "20140321",
      "center_classification_date": "20140528",
      "termination_date": "20141114",
      "report_date": "20140604",
      "code_info": "508004, exp. 4/2015, NDC 51285-204-01, Single Unit  508004, exp. 4/2015, NDC 51285-204-02, Carton of 5 Units",
      "more_code_info": ""
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}