{
  "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": "Ocala",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "75289",
      "recalling_firm": "Wells Pharmacy Network LLC",
      "address_1": "1210 SW 33rd Ave",
      "address_2": "N/A",
      "postal_code": "34474-2853",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0337-2017",
      "product_description": "Alprostadil 20 mcg/mL Injectable, a) 5 mL  and b) 10 mL vials, Compounded by Wells Pharmacy Network LLC, Ocala FL",
      "product_quantity": "a) 24 vials, b) 91 vials",
      "reason_for_recall": "Lack of Assurance of Sterility",
      "recall_initiation_date": "20160921",
      "center_classification_date": "20170104",
      "termination_date": "20210702",
      "report_date": "20170111",
      "code_info": "All lot codes of product prepared between 02/22/2016 and 09/14/2016, within expiry.     a) Known lot code: 03312016@6  b) Known lot code: 04222016@8, 15202016@85, 06302016@4, 08012016@32"
    }
  ]
}