{
  "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 Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77077",
      "recalling_firm": "CareFusion 303, Inc.",
      "address_1": "10020 Pacific Mesa Blvd",
      "address_2": "N/A",
      "postal_code": "92121-4386",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and to the countries of :  Europe, Australia, New Zealand,  South Africa, Greater Asia, Middle East, and Canada.",
      "recall_number": "Z-2671-2017",
      "product_description": "Alaris PC Unit, Model 8015",
      "product_quantity": "568,283 units",
      "reason_for_recall": "BD initiated the recall of Alaris PC unit model 8015 after the firm identified five scenarios which can result in the occurrence of Systems Error Code 255-16-275 and can potentially result in interrupted infusions.",
      "recall_initiation_date": "20170612",
      "center_classification_date": "20170703",
      "termination_date": "20181026",
      "report_date": "20170712",
      "code_info": "Notification will be distributed to all Alaris PC Unit model 8015 customers with software versions greater than 9.12."
    }
  ]
}