{
  "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": "2026-07-22",
    "results": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Benton",
      "state": "AR",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "96328",
      "recalling_firm": "One Source Nutrition, Inc,",
      "address_1": "19863 Interstate 30 S",
      "address_2": "N/A",
      "postal_code": "72015-6966",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide in the U.S.A",
      "recall_number": "D-0281-2025",
      "product_description": "Vitality, Fast Acting Male Enhancement Product, Dietary Supplement, a) One Capsule per Packet, b) 6 capsules per bottle, Xtreme Potency.",
      "product_quantity": "a) 300 individually wrapped capsules b) 20 bottles",
      "reason_for_recall": "Marketed without an approved NDA/ANDA: Product found to be tainted with undeclared sildenafil and tadalafil.",
      "recall_initiation_date": "20250220",
      "center_classification_date": "20250317",
      "report_date": "20250326",
      "code_info": "All lots"
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