{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Hacienda Heights",
      "state": "CA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Food",
      "event_id": "65733",
      "recalling_firm": "Healthmaxx Global Inc.",
      "address_1": "16231 Elza Dr.",
      "address_2": "N/A",
      "postal_code": "91745",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "CA, MD, and NY",
      "recall_number": "F-1934-2013",
      "product_description": "MAX Brand Nitric Oxide Enhance, 90 Count Capsules    Product labeling reads in part:\"MAX Nitric Oxide Enhance***DIETARY SUPPLEMENT 90 Capsules***0 65176 55958 5***Manufactured in FDA Approved Facility for:HealthMax Products Co. Altadena, CA 91001***\".",
      "product_quantity": "5,223 bottles",
      "reason_for_recall": "In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.",
      "recall_initiation_date": "20130610",
      "center_classification_date": "20130924",
      "termination_date": "20141114",
      "report_date": "20131002",
      "code_info": "Lot # R1018  UPC 0 65176 55958 5"
    }
  ]
}