{
  "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": [
    {
      "status": "Terminated",
      "city": "Lake Forest",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68658",
      "recalling_firm": "Hospira Inc.",
      "address_1": "275 N Field Dr",
      "address_2": "",
      "postal_code": "60045-2579",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide in the states of FL, LA, PA, WA, WY and the country of  Hong Kong",
      "recall_number": "Z-2027-2014",
      "product_description": "The Hospira MedNet Medication Management Suite (MMS).    Product Usage:  The Hospira MedNet Medication Management Suite (MMS) is intended to facilitate networked communication between MMS compatible computer systems and Hospira infusion pumps. The MMS provides trained healthcare professionals with the capability to send, receive, report, and store information from interfaced external systems, and to configure and edit infusion programming parameters. The MMS is intended to provide a way to automate the programming of infusion parameters, thereby decreasing the amount of manual steps necessary to enter infusion data. All data entry and validation of infusion parameters is performed by a trained healthcare professional according to physician\u0019s orders.",
      "product_quantity": "13 units",
      "reason_for_recall": "Hospira MedNet 5.5, 5.8.1, and 5.8.2 contains software defect where the dosing units of \"nanog/kg/min\" and \"milliUnits/min\" are not sent to a Plum A+ device (Version 13.40, 13.41, and 13.4.2) via Auto Programming when those dosing units are not properly established in the customized drug library. A dosing unit mismatch of \"nanog/kg/min\" or \"milliUnits/min\" on an unmatched medication will produce a",
      "recall_initiation_date": "20140606",
      "center_classification_date": "20140709",
      "termination_date": "20161206",
      "report_date": "20140716",
      "code_info": "1) Software Version 5.5, List Number: 16037-04-13;   2) Software Version 5.8.1, List Number: 16037-04-31;   3) Software Version 5.8.2, List Number: 16037-04-33",
      "more_code_info": ""
    }
  ]
}