{
  "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": "2026-07-29",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "status": "Terminated",
      "city": "Doral",
      "state": "FL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "90675",
      "recalling_firm": "Distributor RFR, LLC.",
      "address_1": "3580 Nw 85th Ct Apt 150",
      "address_2": "N/A",
      "postal_code": "33122-1986",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Retail stores in the state of FL, Nationwide in the USA, France and Canada via website sales, and Bolivarian Republic of Venezuela",
      "recall_number": "D-1333-2022",
      "product_description": "SANGTER Energy Supplement Capsules, 3000mg x 7 grain, 7-count blister pack within a carton, Distributed by: Distributor RFR, LLC, (800) 519-0204 Miami 33172 FL, USA; UPC 0 705632 523285",
      "product_quantity": "2000 cartons",
      "reason_for_recall": "Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be tainted with sildenafil.",
      "recall_initiation_date": "20220722",
      "center_classification_date": "20220809",
      "termination_date": "20250729",
      "report_date": "20220810",
      "code_info": "Lot: 48656, Exp. 01/2025"
    }
  ]
}