{
  "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,
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "Williamston",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83584",
      "recalling_firm": "Centurion Medical Products Corporation",
      "address_1": "100 Centurion Way",
      "address_2": "N/A",
      "postal_code": "48895-9086",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide domestic distribution.",
      "recall_number": "Z-0103-2020",
      "product_description": "IV SECUREMENT KIT  IVS3405",
      "product_quantity": "181965 total",
      "reason_for_recall": "Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.",
      "recall_initiation_date": "20190424",
      "center_classification_date": "20191009",
      "termination_date": "20200403",
      "report_date": "20191016",
      "code_info": "2019031490  2017100690  2017110790  2018011790  2018050490  2018060590  2018072490  2018110190  2019011490  2019020690"
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