{
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    "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": "2026-07-29",
    "results": {
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      "status": "Terminated",
      "city": "Diamond Bar",
      "state": "CA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "91711",
      "recalling_firm": "Volt Candy Wholesale Club",
      "address_1": "324 S Diamond Bar Blvd",
      "address_2": "#212",
      "postal_code": "91765-1607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Nationwide in the USA",
      "recall_number": "D-0453-2023",
      "product_description": "PrimeZEN Black 6000 capsule, 2000mg, Male Sexual Performance Enhancement, 1-count blister card, Distributed by: Prime Premier Group, Los Angeles, CA 90006, UPC 7 28175 52189 1.",
      "product_quantity": "432 capsules",
      "reason_for_recall": "Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.",
      "recall_initiation_date": "20230213",
      "center_classification_date": "20230309",
      "termination_date": "20240820",
      "report_date": "20230308",
      "code_info": "Lot number: NPINPB 1003, Expiration date: 08/16/2025",
      "more_code_info": ""
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