{
  "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": "San Clemente",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71028",
      "recalling_firm": "ICU Medical, Inc.",
      "address_1": "951 Calle Amanecer",
      "address_2": "N/A",
      "postal_code": "92673-6212",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in US: SC, NC, MN, CT, KY, MD, FL, VA, TN",
      "recall_number": "Z-1594-2015",
      "product_description": "98\" (249 cm) Transfer Set w/MicroClave T-Connector, Check Valve, Anti-Siphon Valve, Trifuse Ext Set w/2 MicroClave, Rotating Luer, Non-DEHP Tubing, Item No. B3338  Product Usage:  IV Administration sets are intended for the infusion and withdrawal of fluids. The devices are provided sterile.",
      "product_quantity": "900 units",
      "reason_for_recall": "ICU Medical is recalling MicroClave T-Connectors because they have potential connection separation issues that could lead to leakage.",
      "recall_initiation_date": "20150420",
      "center_classification_date": "20150507",
      "termination_date": "20151124",
      "report_date": "20150513",
      "code_info": "Lot No.  2997914  2997918  2998570  3001230  3001231"
    }
  ]
}