{
  "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,
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  "results": [
    {
      "status": "Terminated",
      "city": "Waterford",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "77465",
      "recalling_firm": "American Pharmaceutical Ingredients LLC",
      "address_1": "6650 Highland Rd Ste 302",
      "address_2": "N/A",
      "postal_code": "48327-1665",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "NY, GA, NV, CA, KY, TX",
      "recall_number": "D-0919-2017",
      "product_description": "ESTRONE USP, packaged in a) 1g bottle (NDC: 58597-8049-2), c) 5g bottle (NDC: 58597-8049-3), d) 25g bottle (NDC: 58597-8049-4), For Prescription Compounding, RX Only, Packed under cGMP conditions by American Pharmaceutical Ingredients, LLC, 6650 Highland Road, Waterford, MI 48327",
      "product_quantity": "1g=1 bottle; 5g=4 bottle; 25g=3 bottles",
      "reason_for_recall": "cGMP Deviations; lack of quality assurance.",
      "recall_initiation_date": "20170417",
      "center_classification_date": "20170615",
      "termination_date": "20180531",
      "report_date": "20170621",
      "code_info": "Lots:  052915-1, 052915-2, exp 5/5/2017"
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}