{
  "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": "Commerce",
      "address_1": "5560 E 61st St",
      "reason_for_recall": "Marketed Without an Approved NDA/ANDA: product may contain undeclared sildenafil, tadalafil and analogues of these FDA approved active ingredients, making them unapproved drugs",
      "address_2": "",
      "product_quantity": "70,000 capsules.",
      "code_info": "Lot# 01MJS0712, Exp 07/15.",
      "center_classification_date": "20130516",
      "distribution_pattern": "Nationwide",
      "state": "CA",
      "product_description": "Mojo nights SUPREME Capsules, 1000 mg, Male Sexual Enhancer, supplied in 1 count blister packs, UPC 610585435915; Distributed By: Mojo Health, Pompano Beach, FL",
      "report_date": "20130522",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Performance Plus Marketing, Inc.",
      "recall_number": "D-337-2013",
      "initial_firm_notification": "Telephone",
      "product_type": "Drugs",
      "event_id": "63916",
      "termination_date": "20131114",
      "more_code_info": "",
      "recall_initiation_date": "20121217",
      "postal_code": "90040-3406",
      "voluntary_mandated": "Voluntary: Firm initiated",
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