{
  "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": "Brea",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76339",
      "recalling_firm": "Radiometer America Inc",
      "address_1": "250 S Kraemer Blvd",
      "address_2": "N/A",
      "postal_code": "92821-6232",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S. distribution to the following; nationwide.    Foreign distribution to the following; Netherlands, China, Czech Republic, Denmark, Germany, Spain, France, Hungary, India, Japan, Poland, South Africa, Singapore, Switzerland, Turkey, Norway, Austria, Italy, Sweden, Finland.",
      "recall_number": "Z-1463-2017",
      "product_description": "The ABL800 Model#:All",
      "product_quantity": "17,522",
      "reason_for_recall": "Reports that the sample type \"cord blood\" has been changed into the two sample types \"cord blood arterial\" and \"cord blood venous.",
      "recall_initiation_date": "20170126",
      "center_classification_date": "20170314",
      "termination_date": "20180220",
      "report_date": "20170322",
      "code_info": "The affected analyzers are serial numbers 393-090R0027N001 to present."
    }
  ]
}