{
  "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": "Ridgeland",
      "address_1": "103 W. Washington Street",
      "reason_for_recall": "Marketed Without An Approved NDA/ANDA: Samples tested by FDA were found to contain sulfoaildenafil, an analogue of sildenafil, an FDA approved drug used in the treatment of male erectile dysfunction, making these products unapproved new drugs.",
      "address_2": "Suite B5",
      "product_quantity": "585,000 Capsules",
      "code_info": "Lot #s: a) 101108, 101009, 101010, 101011; b) 101108, 101109, 101110; c) 301000, 301001",
      "center_classification_date": "20120820",
      "distribution_pattern": "Nationwide",
      "state": "MS",
      "product_description": "V Maxx Rx, All Natural Male Enhancement, a) 1-count blister pack UPC Code 2802803561; b) 5-count blister pack UPC Code 0972859402; c) 10-count bottle UPC code 0913251017 bottles, Manufactured by The Menz Club, LLC, 103 W. Washington Street, Suite B5, Ridgeland, MS  39157, Phone: 601-866-6746",
      "report_date": "20120829",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "The Menz Club, LLC",
      "recall_number": "D-1657-2012",
      "initial_firm_notification": "Press Release",
      "product_type": "Drugs",
      "event_id": "61957",
      "termination_date": "20151207",
      "recall_initiation_date": "20120525",
      "postal_code": "39157",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}