{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Amityville",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Food",
      "event_id": "66765",
      "recalling_firm": "Global Health Laboratories, LLC",
      "address_1": "9500 New Horizons Blvd",
      "address_2": "N/A",
      "postal_code": "11701-1155",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "New York",
      "recall_number": "F-1105-2014",
      "product_description": "UT-Fem¿ FOR WOMEN, urinary tract SOLUTION, Dietary Supplement, 42 Vegetable Capsules, Product No. 110403, UPC 7 98304 24865 4 -- Manufactured for: Global Quality Health Inc.",
      "product_quantity": "1495 bottles",
      "reason_for_recall": "The finished dietary supplement product was manufactured with ingredients subsequently found to be contaminated with chloramphenicol, an antibiotic, at levels above 0.3 ppb.  The supplier, Specialty Enzymes & Biotechnologies, recalled the raw materials and notified the recipients.  Subsequent private laboratory testing of the finished product revealed levels of chloramphenicol above 0.3 ppb.",
      "recall_initiation_date": "20131107",
      "center_classification_date": "20131218",
      "termination_date": "20170308",
      "report_date": "20131225",
      "code_info": "Lot Number 1256074"
    }
  ]
}