{
  "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": "Saint Paul",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66987",
      "recalling_firm": "Smiths Medical ASD, Inc.",
      "address_1": "1265 Grey Fox Rd",
      "address_2": "N/A",
      "postal_code": "55112-6929",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide ) including the states of : AZ, NY, TN, MS, AR, WV, VA, VT, PA, DE, DC, OH, CO, NH, MI, CA, FL, CT, WA, MD, NM, RI, MA, TX, NC, IL, KY, WI and MI., and the countries of CANADA, SAUDI ARABIA and AUSTRALIA.",
      "recall_number": "Z-0540-2014",
      "product_description": "Medfusion¿ 4000 Syringe Infusion Pumps    Medfusion¿ 4000 Syringe Infusion Pumps are designed for use in care areas for the administration of fluids requiring precisely controlled infusion rates. These pumps are indicated for use by healthcare professionals in the delivery of IV solutions, drug solutions, blood or blood products, and enteral feedings in continuous, intermittent, and body weight delivery modes.",
      "product_quantity": "9560 (8601 US, 959 OUS)",
      "reason_for_recall": "Smiths Medical is conducting a recall involving  all Medfusion¿ 4000 Syringe Infusion Pumps.  Smiths Medical has identified an issue with electrical shorting at the AC power receptacle. Shorting can occur when saline solution or other conductive fluids (e.g., potassium chloride) enter the AC power receptacle. When this happens, sparking and/ or flames, accompanied by smoke, may appear at the AC po",
      "recall_initiation_date": "20131122",
      "center_classification_date": "20131219",
      "termination_date": "20150325",
      "report_date": "20131225",
      "code_info": "All Medfusion¿ 4000 Syringe Pumps in the field are affected by this Field Safety Corrective Action."
    }
  ]
}