{
  "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
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  },
  "results": [
    {
      "country": "United States",
      "city": "Boca Raton",
      "address_1": "1140 Holland Dr",
      "reason_for_recall": "Marketed without an approved NDA/ANDA: product label states it contains anabolic steroids.",
      "address_2": "Ste 12",
      "product_quantity": "1250 bottles",
      "code_info": "All lots remaining within expiry.",
      "center_classification_date": "20170912",
      "distribution_pattern": "Florida",
      "state": "FL",
      "product_description": "ANDROPHARM M1 ALPHA (Methyl-1-Etiocholenolol-Epietiocholanollone 20 mg) capsule, packaged in 60-count bottle, Amazon.com,  UPC 6 42125 50292 4",
      "report_date": "20170920",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Andropharm, LLC",
      "recall_number": "D-1143-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "77664",
      "termination_date": "20200602",
      "recall_initiation_date": "20170606",
      "postal_code": "33487-2764",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}