{
  "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": {
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  "results": [
    {
      "country": "United States",
      "city": "Oklahoma City",
      "address_1": "755 Research Pkwy Ste 150",
      "reason_for_recall": "Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.",
      "address_2": "",
      "product_quantity": "unknown",
      "code_info": "all lot codes",
      "center_classification_date": "20140729",
      "distribution_pattern": "Nationwide",
      "state": "OK",
      "product_description": "Dermamedics Post Procedure Cream, 1 ounce containers which were distributed with a SKU number of DM 1026",
      "report_date": "20140806",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Dermamedics, L.L.C.",
      "recall_number": "D-1487-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "67247",
      "termination_date": "20170314",
      "more_code_info": "",
      "recall_initiation_date": "20140110",
      "postal_code": "73104-3621",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}