{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Irvine",
      "address_1": "2 Park Plaza",
      "reason_for_recall": "The firm is recalling all herbal and dietary supplements because they were not manufactured in compliance with the current Good Manufacturing Practice regulations for Dietary Supplements.",
      "address_2": "Suite 1200",
      "product_quantity": "4000 units",
      "code_info": "Lot AAMXG",
      "center_classification_date": "20170331",
      "distribution_pattern": "US",
      "state": "CA",
      "product_description": "RegeneSlim",
      "report_date": "20170412",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "VivaCeuticals, Inc. dba Regeneca Worldwide",
      "recall_number": "F-1819-2017",
      "initial_firm_notification": "Press Release",
      "product_type": "Food",
      "event_id": "76634",
      "termination_date": "20170808",
      "recall_initiation_date": "20170309",
      "postal_code": "92614-2562",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}