{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Minneapolis",
      "state": "MN",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80632",
      "recalling_firm": "Smiths Medical ASD Inc.",
      "address_1": "6000 Nathan Ln N",
      "address_2": "N/A",
      "postal_code": "55442-1690",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution in the states of  CT, MA, MI, NC, NJ, NY, RI, TX, UT, and WA.",
      "recall_number": "Z-3196-2018",
      "product_description": "Portex Pulsator Arterial Blood Sampling Kit with Dry Lithium Heparin for Gases and Electrolytes, REF 4080P-2, Sterile, RX.  The firm name on the label is Smiths Medical ASD, Inc., Keene, NH.",
      "product_quantity": "29,600 kits",
      "reason_for_recall": "The product was mislabeled with the incorrect label.",
      "recall_initiation_date": "20180713",
      "center_classification_date": "20180918",
      "termination_date": "20181019",
      "report_date": "20180926",
      "code_info": "Lot numbers 3306404, 3314069, and 3318698."
    }
  ]
}