{
  "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": "Powell",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69782",
      "recalling_firm": "Pulsion Medical Inc",
      "address_1": "3781 Attucks Dr",
      "address_2": "",
      "postal_code": "43065-6080",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution in the states of CT, NJ and NY. The affected product was distributed to one government consignee.",
      "recall_number": "Z-1121-2015",
      "product_description": "Pulsiocath PiCCO ProAQT Monitoring Kit, single-use cardiac output (CO) sensor, one unit per plastic sterilizable package.     Product Usage:  Measures cardiac output by the thermodilution method, measurement of arterial blood pressure, and for cardiac output determination by arterial pulse contour analysis.",
      "product_quantity": "90 units",
      "reason_for_recall": "Internal testing and investigation of the packaging revealed cracks and holes in primary packaging",
      "recall_initiation_date": "20141104",
      "center_classification_date": "20150217",
      "termination_date": "20151002",
      "report_date": "20150225",
      "code_info": "Model Number PV8810US; Lot # 14AK20 and 14EK20",
      "more_code_info": ""
    }
  ]
}