{
  "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": "2026-07-08",
    "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": "96188",
      "recalling_firm": "MEDLINE INDUSTRIES, LP - Northfield",
      "address_1": "3 Lakes Dr",
      "address_2": "N/A",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US States: CA, NY",
      "recall_number": "Z-1182-2025",
      "product_description": "Medline Convenience Kits for Various Procedures:  1) ADULT INTUBATION TRAY, Model Number DYNJAA254A;  2) ADULT MAIN DISP. INTUB PART A, Model Number DYNJAA262A",
      "product_quantity": "70 kits",
      "reason_for_recall": "Kits contain recalled components due to reports of reduced skin barrier wear time. This refers to a shorter duration that a skin barrier can effectively adhere to and protect the skin before it needs to be replaced.",
      "recall_initiation_date": "20250109",
      "center_classification_date": "20250219",
      "report_date": "20250226",
      "code_info": "1) DYNJAA254A, UDI-DI 10195327686260 (each) 40195327686261 (case), Lot Number   24KBR956, 24LBA655; 2) DYNJAA262A, UDI-DI 10195327208172 (each) 40195327208173 (case), Lot Number 24LBD397"
    }
  ]
}