{
  "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-1938-2013",
      "product_description": "MAX Brand RESVERATROL, 120 Count Capsules.    Product labeling reads in part:\"MAX RESVERATROL***Dietary Supplement 120 CAPSULES***Manufactured in FDA Approved Facility for:HealthMax Products Inc. Altadena, CA 91001***0 65176 30325 6\".",
      "product_quantity": "2,659 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 # A0830  UPC 0 65176 30325 6"
    }
  ]
}