{
  "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": "Nixa",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80317",
      "recalling_firm": "SPS Sterilization, Inc",
      "address_1": "1110 N Gerald St",
      "address_2": "N/A",
      "postal_code": "65714-7445",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US distribution to AZ, CA, FL, OH, PA, TX, VA, WV",
      "recall_number": "Z-3041-2018",
      "product_description": "Vascular Solutions Venture Rx Catheter, 6F, resterilized.",
      "product_quantity": "3 units total",
      "reason_for_recall": "The expiration date on the device labeling exceeds its actual validated shelf life because the sterilization process used does not have adequate support for the extended shelf life.",
      "recall_initiation_date": "20180307",
      "center_classification_date": "20180913",
      "termination_date": "20181127",
      "report_date": "20180919",
      "code_info": "Code Number 5820-R; Lot Number 570183 (Serial Number 99804132016-07); Lot Number 583022 (Serial Number 17304202017-07, 17304202017-08)"
    }
  ]
}