{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Northfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86423",
      "recalling_firm": "Medline Industries Inc",
      "address_1": "3 Lakes Dr",
      "address_2": "N/A",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "62 US consignees; 1 government consignee, 4 foreign consignees",
      "recall_number": "Z-0058-2021",
      "product_description": "ClearPro Closed Suction Catheter, Model DYNCPDS14T, 14 Fr  FOR ENDOTRACHEAL TUBE - Product Usage: Catheters are intended for endotracheal suction of adult patients with artificial airways. Single use only.",
      "product_quantity": "6225 units",
      "reason_for_recall": "There have been reports of the suction catheter coming apart from the device assembly during use.",
      "recall_initiation_date": "20200901",
      "center_classification_date": "20201006",
      "termination_date": "20220527",
      "report_date": "20201014",
      "code_info": "Model: DYNCPDS14T, Lots 06919010016 and 06919020016"
    }
  ]
}