{
  "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": "Sanford",
      "state": "FL",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "67420",
      "recalling_firm": "Hill Dermaceuticals, Inc.",
      "address_1": "2650 S Mellonville Ave",
      "address_2": "N/A",
      "postal_code": "32773-9311",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide and Puerto Rico",
      "recall_number": "D-1181-2014",
      "product_description": "SETON PHARMACEUTICALS Fluocinolone Acetonide 0.01%  Oil EAR DROPS, 20 ml, Rx only Manufactured by: Hill Dermaceuticals, Inc. For:  Seton Pharmaceuticals NDC 13925-508-20",
      "product_quantity": "13,591 bottles",
      "reason_for_recall": "Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.",
      "recall_initiation_date": "20140131",
      "center_classification_date": "20140324",
      "termination_date": "20150203",
      "report_date": "20140402",
      "code_info": "13F017B exp. 12/14, 13F020B exp 12/14"
    }
  ]
}