{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "San Marcos",
      "state": "TX",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "77660",
      "recalling_firm": "HARDCORE FORMULATIONS",
      "address_1": "3012 Fm 621 Ste B",
      "address_2": "N/A",
      "postal_code": "78666-1668",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-1084-2017",
      "product_description": "ULTRA-STEN Rapid Size and Strength capsules, 10 mgs, 90 count bottle, Hardcore Formulations UPC: 7 48252 68763 0",
      "product_quantity": "1490 bottles",
      "reason_for_recall": "Marketed Without An Approved NDA/ANDA: Product contains Methylstenbolone or Dymethazine.",
      "recall_initiation_date": "20170705",
      "center_classification_date": "20170814",
      "termination_date": "20201005",
      "report_date": "20170823",
      "code_info": "All lots remaining within expiry."
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}