{
  "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": "2026-04-22",
    "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": "62538",
      "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 distribution",
      "recall_number": "Z-2131-2012",
      "product_description": "Flush Kit w 3 Way Off Stopcock    Product Usage:  Flush Kit",
      "product_quantity": "N/A",
      "reason_for_recall": "The firm initiated the recall due to a molding defect in a high pressure stopcock where a small  percentage of the side ports could become totally occluded.",
      "recall_initiation_date": "20120417",
      "center_classification_date": "20120802",
      "termination_date": "20120823",
      "report_date": "20120808",
      "code_info": "Part Number AG8137  510(k) K052865  Lot number 2466161"
    }
  ]
}