{
  "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": "2026-07-29",
    "results": {
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  "results": [
    {
      "status": "Terminated",
      "city": "North Tonawanda",
      "state": "NY",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "89462",
      "recalling_firm": "CooperSurgical, Inc",
      "address_1": "825 Wurlitzer Dr",
      "address_2": "N/A",
      "postal_code": "14120-3041",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide",
      "recall_number": "D-0643-2022",
      "product_description": "PARAGARD T380A (intrauterine copper contraceptive), 1 unit per carton together with an insertion tube and solid white rod in a Tyvek polyethylene pouch, Rx Only, Manufactured by Teva Women's Health Inc. a subsidiary of Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 51285-204-01",
      "product_quantity": "48,645 cartons",
      "reason_for_recall": "Non-sterility",
      "recall_initiation_date": "20220204",
      "center_classification_date": "20220301",
      "termination_date": "20230206",
      "report_date": "20220223",
      "code_info": "Lot # 517001,Exp 1/2024"
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}