{
  "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": "Moses Lake",
      "state": "WA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "71806",
      "recalling_firm": "JD & SN Inc., dba Moses Lake Professional Pharmacy",
      "address_1": "1555 Pilgrim St",
      "address_2": "N/A",
      "postal_code": "98837-4623",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0079-2016",
      "product_description": "ESTRADIOL, Pellet, 12 mg, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA  98837, (509)764-2314",
      "product_quantity": "1 pellet",
      "reason_for_recall": "Lack of Assurance of Sterility; all sterile human compounded drugs within expiry",
      "recall_initiation_date": "20150724",
      "center_classification_date": "20151027",
      "termination_date": "20160413",
      "report_date": "20151104",
      "code_info": "07102015@10"
    }
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}