{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Northfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78319",
      "recalling_firm": "Medline Industries Inc",
      "address_1": "Three Lakes Drive",
      "address_2": "N/A",
      "postal_code": "60093",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "FL, IN, TN, GA, NJ, UT, MD,  Nicaragua, Honduras",
      "recall_number": "Z-0112-2018",
      "product_description": "MEDLINE PEDI ELBOW CLOSED SUCTION CATHETER, 8Fr, REF DYNCPE8",
      "product_quantity": "190 units",
      "reason_for_recall": "Products labeled as sterile were distributed prior to sterilization",
      "recall_initiation_date": "20171010",
      "center_classification_date": "20171118",
      "termination_date": "20200804",
      "report_date": "20171129",
      "code_info": "Lot 2861707008"
    }
  ]
}