{
  "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": "Hospira has received customer reports of broken door assemblies on the Hospira/Abbott Acclaim Encore infusion pumps. If the door assembly breaks, it may prevent the door from closing properly and unrestricted flow may occur. If the door cannot be closed, the pump cannot be used which can  result in a delay in therapy.",
      "address_2": "",
      "product_quantity": "13,218 infusion pumps total",
      "code_info": "List Number: 12032;   Serial Numbers: 12322921,  12323859,  12322780,  12322801,  12322810,  12322812,  12322878,  12322880,  12322887,  12322896,  12322903,  12322904,  12322911,  12322917,  12322936,  12322939,  12323867,  12322916,  12323056,  12321139,  12324767,  12324854,  12324802,  12322873,  12324375,  1231453,  1231610.",
      "center_classification_date": "20140501",
      "distribution_pattern": "Nationwide Distribution -- AK, AL, AR, AZ, CA, CO, CR, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, and WY.",
      "state": "IL",
      "product_description": "Abbott Acclaim Infusion Pump    Designed to deliver parenteral infusions including whole blood or red blood cell components and enteral fluids using a wide variety of standard administration sets and fluid containers.",
      "report_date": "20140507",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Hospira Inc.",
      "recall_number": "Z-1482-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67591",
      "termination_date": "20170816",
      "more_code_info": "",
      "recall_initiation_date": "20131031",
      "postal_code": "60045-2579",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}