{
  "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": [
    {
      "country": "United States",
      "city": "San Diego",
      "address_1": "10020 Pacific Mesa Blvd",
      "reason_for_recall": "During an infusion, a false Air-in-Line (AIL) alarm would cause the infusion to be interrupted.",
      "address_2": "",
      "product_quantity": "382,635 units",
      "code_info": "All products manufactured or serviced in the time period October 2011 through June 2015.",
      "center_classification_date": "20170118",
      "distribution_pattern": "Nationwide Distribution",
      "state": "CA",
      "product_description": "Alaris Pump Module, Model No. 8100 and AIL sensor kits, P/N 147083-102 and P/N 49000221.    The Alaris Pump module is a large volume infusion pump offered under the Alaris System. The Alaris Pump module will deliver medication and fluids using IV administration sets for continuous or intermittent delivery through clinically acceptable routes of administration such as intravenous or epidural",
      "report_date": "20170125",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "CareFusion 303, Inc.",
      "recall_number": "Z-0950-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75466",
      "termination_date": "20180724",
      "more_code_info": "",
      "recall_initiation_date": "20161202",
      "postal_code": "92121-4386",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}