{
  "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": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Princeton",
      "state": "NJ",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "97031",
      "recalling_firm": "Church & Dwight Inc",
      "address_1": "469 N Harrison St",
      "address_2": "",
      "postal_code": "08540-3510",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Nationwide in the USA.",
      "recall_number": "D-0504-2025",
      "product_description": "ZICAM COLD REMEDY MEDICATED NASAL SWABS, 20 Single-Use Swabs per carton, Distributed by Church & Dwight Co,. Inc., Ewing NJ. UPC 7 32216 30120 5",
      "product_quantity": "3,374,918 cartons",
      "reason_for_recall": "Microbial Contamination of Non-Sterile Products: Fungal contamination of nasal swabs.",
      "recall_initiation_date": "20250606",
      "center_classification_date": "20250703",
      "report_date": "20250709",
      "code_info": "All lots.",
      "more_code_info": ""
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}