{
  "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": "Minneapolis",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81599",
      "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": "E-Mail",
      "distribution_pattern": "The potentially affected products were shipped to customers in the US, Canada, and Mexico.",
      "recall_number": "Z-0512-2019",
      "product_description": "Medex High Pressure Stopcock used to control the direction of IV fluid flow. This device is intended for single use only and is provided sterile and fluid path non-pyrogenic unless package is damaged or opened.",
      "product_quantity": "2,425 devices",
      "reason_for_recall": "Certain lots of Medex\" High Pressure Stopcocks were manufactured with an inner body defect that may result in a leak.    Model Number - Lot Number  MX4301L - 3538569  MX4331L - 3562377 & 3546826  MX4331R - 3546924",
      "recall_initiation_date": "20181119",
      "center_classification_date": "20181128",
      "termination_date": "20200605",
      "report_date": "20181205",
      "code_info": "Model Number (Lot Number):  MX4301L (3538569), MX4331L (3562377, 3546826), MX4331R (3546924)"
    }
  ]
}