{
  "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": {
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  "results": [
    {
      "country": "United States",
      "city": "Roscoe",
      "address_1": "5062 Rock Rose Ct.",
      "reason_for_recall": "Marketed Without An Approved NDA/ANDA: FDA analysis found the product to contain hydroxythiohomosildenafil, an analogue of sildenafil which is an ingredient in an FDA-approved drug for the treatment of male erectile dysfunction, making this an unapproved new drug.",
      "address_2": "Suite #40",
      "product_quantity": "11,424 blister packs",
      "code_info": "All product sold between 01/01/13 through 03/27/13.",
      "center_classification_date": "20130516",
      "distribution_pattern": "Nationwide",
      "state": "IL",
      "product_description": "ROCK-IT MAN capsules, male sexual stimulant, packaged in 1-count (UPC 8 53447 02003 8) and 2-count (UPC 8 53447 00204 1) blister cards, Distributed by Consumer Concepts.",
      "report_date": "20130522",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Consumer Concepts, Inc.",
      "recall_number": "D-325-2013",
      "initial_firm_notification": "E-Mail",
      "product_type": "Drugs",
      "event_id": "64838",
      "termination_date": "20180510",
      "more_code_info": "",
      "recall_initiation_date": "20130401",
      "postal_code": "61073",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}