{
  "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": "2026-07-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Pittsford",
      "state": "NY",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "65095",
      "recalling_firm": "American Lifestyle.Com",
      "address_1": "640 Kreag Rd Ste 101",
      "address_2": "N/A",
      "postal_code": "14534-3737",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Domestic distribution currently under Investigation; International distribution includes, but may not be limited to the following countries : Mexico, France, Brazil, Belgium, Denmark, Switzerland, Spain, Canada, Italy, Japan, Ireland, Venezuela, Oman.",
      "recall_number": "D-1224-2014",
      "product_description": "Black Ant, 4600 mg x 4.  Product is packaged in a small green box with gold lettering on the front, the back side of the box contains mostly foreign character.  Within the box there are four (4) capsules individually wrapped in black and red plastic with white lettering.  UPC 4026666142546 (product numbers may possibly vary for same product identification and same product packaging).",
      "product_quantity": "3 boxes distributed domestically & 4 boxes distributed internationally to consumers.",
      "reason_for_recall": "Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the FDA has determined the Vicerex product contains undeclared tadalafil and the Black Ant product contains undeclared sildenafil.   Tadalafil and sildenafil are FDA-Approved drugs used to treat male erectile dysfunction (ED), making the Vicerex and the Black Ant products unapproved new drugs.",
      "recall_initiation_date": "20130430",
      "center_classification_date": "20140407",
      "termination_date": "20180627",
      "report_date": "20140416",
      "code_info": "All lots, UPC 4026666142546."
    }
  ]
}