{
  "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": [
    {
      "status": "Terminated",
      "city": "Maple Grove",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80135",
      "recalling_firm": "Vascular Solutions, Inc.",
      "address_1": "6464 Sycamore Ct N",
      "address_2": "N/A",
      "postal_code": "55369-6032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-2249-2018",
      "product_description": "Drainer(R) Centesis Catheters:  (a) REF 8810, 5F x 9cm  (b) REF 8811, 6F x 9cm  (c) REF 8812, 5F x 15cm    Product The Drainer centesis catheter is intended for use in percutaneous fluid aspirations and small volume drainage procedures.",
      "product_quantity": "276 units",
      "reason_for_recall": "The supplier of Drainer(R) centesis catheters notified Vascular Solutions, Inc. that there is a potential for certain production lots to contain unsafe levels of bacterial endotoxins.",
      "recall_initiation_date": "20180504",
      "center_classification_date": "20180618",
      "termination_date": "20201005",
      "report_date": "20180627",
      "code_info": "a) REF 8810, 5F x 9cm, Lot Numbers:  18037128, 18057123  (b) REF 8811, 6F x 9cm, Lot Numbers:  18026062, 18026063  (c) REF 8812, 5F x 15cm, Lot Number:  18050076"
    }
  ]
}