{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "94387",
      "product_res_number": "Z-0126-2011",
      "event_date_initiated": "2010-07-26",
      "event_date_posted": "2010-10-22",
      "recall_status": "Terminated",
      "event_date_terminated": "2014-02-25",
      "res_event_number": "56730",
      "product_code": "DNN",
      "product_description": "EndoTool Drug Dose Calculator-Software Version 7.2.1800.3 and 7.2.1825.5",
      "code_info": "Software Version 7.2.1800.3 and 7.2.1825.5",
      "firm_fei_number": "3013319212",
      "recalling_firm": "Hospira, Inc.",
      "address_1": "600 N Field Dr Bldg J45 600 N Field Dr",
      "address_2": "Bldg J45",
      "city": "Lake Forest",
      "state": "IL",
      "postal_code": "60045",
      "additional_info_contact": "Ileana Quinones\n224-212-4892",
      "reason_for_recall": "The EndoTool software did not always provide an audible alert when a blood glucose measurement was due. This could result in a patient not receiving an appropriate dose of insulin.",
      "root_cause_description": "Other",
      "action": "Hospira issued an Urgent Device Field Correction letter dated July 23, 2010 to consignees, providing details of the potential issue and the associated patient risk. Hospira is finalizing software enhancements which will resolve this situation within the next 90 days ,and will contact each consignee when it is available to be downloaded from the Hospira website. The notification letter also included a clinical bulletin, outlining mitigation instructions for clinicians to use until the software enhancement is available. Consignees were requested to complete and return an attached Reply Form by fax.\nCustomers can contact the Hospira EndoTool support line at 1-877-349-4582 for clinical inquiries about this recall.",
      "product_quantity": "97 units total (96 version 7.2.1800.3 and 1 version 7.2.1825.5)",
      "distribution_pattern": "Nationwide Distribution in states of CA, FL, IL, IN, KY, KS, MI, MO, MT, NC, NJ, NM, NV, OH, SC, SD, TN, TX, VA, WA, and WY.",
      "openfda": {
        "k_number": [
          "K853532",
          "K990516",
          "K924733",
          "K810466",
          "K973054",
          "K802620",
          "K882117"
        ],
        "registration_number": [
          "3003951180",
          "1319681",
          "3005333358",
          "2050010",
          "2030861",
          "3032147516",
          "1319808",
          "2020952",
          "2050012",
          "1221645",
          "3003610499",
          "3010939897",
          "1827821",
          "2250051"
        ],
        "fei_number": [
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          "3003951180",
          "3005333358",
          "2050010",
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          "3032147516",
          "2020952",
          "2050012",
          "1000305841",
          "1221645",
          "3003610499",
          "3010939897",
          "1827821",
          "2250051"
        ],
        "device_name": "Calibrators, Ethyl Alcohol",
        "medical_specialty_description": "Clinical Toxicology",
        "regulation_number": "862.3200",
        "device_class": "2"
      }
    }
  ]
}