{
  "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": "Lake Forest",
      "address_1": "275 N Field Dr",
      "reason_for_recall": "There is the potential for the door roller assembly on the Plum LifeCare 5000 Series and Plum XL families of infusers to break. In the event of a broken door roller pin, the door cannot appropriately lock the cassette in the right position. Depending on the conditions of a broken door roller pin, a number of events can occur. The door cannot be closed or a cassette/door alarm or a false occlusion",
      "address_2": "",
      "product_quantity": "List Number 02507: 132,889 pumps",
      "code_info": "List Number: 02507; Serial Numbers: All.",
      "center_classification_date": "20140603",
      "distribution_pattern": "Worldwide Distribution - USA nationwide including District of Columbia, Puerto Rico, and US Virgin Islands; Australia, Argentina, Bahrain, Belgium, Bosnia and Herzegovina, Brazil, Bulgaria, Canada, Chile, Colombia, Croatia, Czech Republic, Egypt, Finland, France, Germany, Greece, Hong Kong, Hungary, Israel, Italy, Jordan, Kuwait, Luxembourg, Mexico, Oman, Peru, Poland, Portugal, Qatar, Russia, San Marino, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, Syria, Taiwan, Turkey, United Arab Emirates, United Kingdom, and Yemen.",
      "state": "IL",
      "product_description": "LifeCare 5000 Pump (Plum 1.6) infusion pump, indicated for  volumetric infusion of critical drugs and fluids by intravenous (I.V.) administration.",
      "report_date": "20140611",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Hospira Inc.",
      "recall_number": "Z-1702-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67453",
      "termination_date": "20161107",
      "more_code_info": "",
      "recall_initiation_date": "20140124",
      "postal_code": "60045-2579",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}