{
  "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": "2026-09-02",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Northfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99506",
      "recalling_firm": "Medline Industries, LP",
      "address_1": "3 Lakes Dr",
      "address_2": "N/A",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide distribution in the state of California.",
      "recall_number": "Z-2999-2026",
      "product_description": "Medline medical convenience kit labeled as:  TRACH TUBE KIT, Medline Kit SKU DYKM2330",
      "product_quantity": "45 kits",
      "reason_for_recall": "Component labeling discrepancy",
      "recall_initiation_date": "20260710",
      "center_classification_date": "20260821",
      "report_date": "20260902",
      "code_info": "UDI/DI 10198459582158 (each) 40198459582159 (case), Lot Number 26FLA408"
    }
  ]
}