{
  "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": "2026-07-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Norwalk",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "92857",
      "recalling_firm": "Ecometics, Inc.",
      "address_1": "19 Concord St",
      "address_2": "N/A",
      "postal_code": "06854-3706",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the USA",
      "recall_number": "D-1102-2023",
      "product_description": "Lugol's (Strong Iodine Solution USP), Each mL contains Iodine 0.05gm and potassium iodide 0.100gm, 8mL Single Use Vials, Rx Only, Manufactured for CooperSurgical, Trumbull, CT  06611, NDC 59365-6064-0, Ref 6064.",
      "product_quantity": "38,486 vials",
      "reason_for_recall": "CGMP Deviations: Products not manufactured under current good manufacturing practices.",
      "recall_initiation_date": "20230809",
      "center_classification_date": "20230824",
      "report_date": "20230830",
      "code_info": "Lot #: 2E235A, exp: 2/2024; 2E293A, exp: 3/2024"
    }
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}