{
  "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,
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  "results": [
    {
      "country": "United States",
      "city": "Melbourne",
      "address_1": "4355 Dow Rd",
      "reason_for_recall": "Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the FDA has determined that J.R.  Jack Rabbit Male Enhancement product was found to contain two undeclared  active pharmaceutical ingredients: sildenafil and tadalafil.",
      "address_2": "D19",
      "product_quantity": "1,000 Tablets",
      "code_info": "Lot #: 2510  Exp 04/01/15",
      "center_classification_date": "20131127",
      "distribution_pattern": "Nationwide",
      "state": "FL",
      "product_description": "J.R.  Jack Rabbit All Natural Herbal Supplement, One tablet can last 24-72 hours, 4-count tablets per blister pack, Order at: www.jackrabbitfourpack.com, Jack Rabbit Inc., 4355 Dow Road, Melbourne, FL 32934",
      "report_date": "20131204",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Jack Rabbit, Inc",
      "recall_number": "D-021-2014",
      "initial_firm_notification": "E-Mail",
      "product_type": "Drugs",
      "event_id": "65895",
      "termination_date": "20201005",
      "recall_initiation_date": "20130812",
      "postal_code": "32934-9220",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}