{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Covington",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72756",
      "recalling_firm": "C.R. Bard, Inc.",
      "address_1": "8195 Industrial Blvd NE",
      "address_2": "N/A",
      "postal_code": "30014-1497",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution-DC and the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI. IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI, and WV.",
      "recall_number": "Z-0760-2016",
      "product_description": "Arctic Sun 5000 and Arctic Sun 2000;  Intended for monitoring and controlling patient temperatures.",
      "product_quantity": "1,539",
      "reason_for_recall": "Improper targeted temperature therapy was delivered to patients because the Temperature Simulator Key was connected to the patient temperature cable instead of the patient temperature probe.",
      "recall_initiation_date": "20151110",
      "center_classification_date": "20160205",
      "termination_date": "20170421",
      "report_date": "20160217",
      "code_info": "All lots/serial numbers sold prior to August 2014.",
      "more_code_info": ""
    }
  ]
}