{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Sanford",
      "address_1": "3875 Saint Johns Pkwy",
      "reason_for_recall": "cGMP Deviations",
      "address_2": "",
      "product_quantity": "Unknown",
      "code_info": "All product within expiry",
      "center_classification_date": "20180406",
      "distribution_pattern": "Nationwide.",
      "state": "FL",
      "product_description": "Conzerol (antipoxin) H2O2 Gel, Hydrogen Peroxide Gel 3%, 1.5 oz. tube, OTC, Manufactured for Elrose Labs, Inc., Sanford, FL",
      "report_date": "20180418",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Elroselabs Inc.",
      "recall_number": "D-0623-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "79606",
      "termination_date": "20201215",
      "more_code_info": "",
      "recall_initiation_date": "20180328",
      "postal_code": "32771-6371",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}