{
  "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": [
    {
      "country": "United States",
      "city": "San Diego",
      "address_1": "10020 Pacific Mesa Blvd",
      "reason_for_recall": "There is a potential risk that could cause unintended flow in the older, centered sear door latch design in the Alaris Pump module model 8100.",
      "address_2": "",
      "product_quantity": "35,940 units",
      "code_info": "Notification will be distributed to all Alaris Pumps customers with pumps manufactured between June 2002 through June 2004.",
      "center_classification_date": "20170707",
      "distribution_pattern": "US and Canada",
      "state": "CA",
      "product_description": "Alaris Pump Module model 8100",
      "report_date": "20170719",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "CareFusion 303, Inc.",
      "recall_number": "Z-2700-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "77279",
      "termination_date": "20190128",
      "more_code_info": "",
      "recall_initiation_date": "20170612",
      "postal_code": "92121-4386",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}