{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Minneapolis",
      "address_1": "6000 Nathan Ln N",
      "reason_for_recall": "The povidone iodine prep pads packaged with the arterial blood sampling kits will not maintain the iodine potency through its labeled 36-month expiration dating.",
      "address_2": "",
      "product_quantity": "Approx. 28,578,939 kits for both products",
      "code_info": "Product with expiration dates between 11/30/2016 and 5/31/2020.",
      "center_classification_date": "20190215",
      "distribution_pattern": "Distribution was nationwide, including Puerto Rico.  There was also military/government distribution.  Foreign distribution was made to Canada, United Arab Emirates, Bahamas, Costa Rica, Latvia, and Saudi Arabia.",
      "state": "MN",
      "product_description": "Aplicare Povidone Iodine Prep Pads packaged within Portex Pro-Vent Arterial Blood Sampling Kit with Dry Lithium Heparin for Gases and Electrolytes, models 4589P-1, 4591EG-1, 4591P-1, 4599P-1, 4611LH, 4611P-1, 4620EG-1, 4620P-1, 4640LH, 4640P-1, 4649P-1, 4660EG-1, 4660P-1, 4699LH, 4699P-1, G1325, G1412, G1481, G1509, G1548, G1581, G1586, G1602, G1627, G1632, G1634, G1671, G1675, G1716, G1724, G1773, and G1807.  The firm name on the label is Smiths Medical ASD, Inc., Keene, NH.",
      "report_date": "20190227",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Smiths Medical ASD Inc.",
      "recall_number": "Z-0842-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "80829",
      "termination_date": "20201005",
      "more_code_info": "",
      "recall_initiation_date": "20180622",
      "postal_code": "55442-1690",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}