{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Racine",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99105",
      "recalling_firm": "Inter-Med Llc",
      "address_1": "2200 South St",
      "address_2": "N/A",
      "postal_code": "53404-1510",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "US Nationwide distribution in the states of Tennessee and Missouri.",
      "recall_number": "Z-2400-2026",
      "product_description": "Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit,  Catalog number 504600-28",
      "product_quantity": "500",
      "reason_for_recall": "Some units of Aluminum Chloride Gel contain the package insert for Ferric Sulfate Gel. The incorrect insert misidentifies the product and contains different first aid instructions, most critically in that the Ferric Sulfate insert instructs users to induce vomiting in the case of ingestion, while the correct Aluminum Chloride insert instructs users not to induce vomiting.",
      "recall_initiation_date": "20260527",
      "center_classification_date": "20260610",
      "report_date": "20260617",
      "code_info": "Model No. 504600-28; UDI-DI 00371347008104; Lot Number 2026-0204"
    }
  ]
}