{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Bloomington",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94395",
      "recalling_firm": "Cook Medical Incorporated",
      "address_1": "400 N Daniels Way",
      "address_2": "N/A",
      "postal_code": "47404-9155",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "International distribution in the countries of Germany, Netherlands, Switzerland, United Kingdom.",
      "recall_number": "Z-1832-2024",
      "product_description": "EchoTip¿ Ultra HD Endoscopic Ultrasound Access Needle, ECHO-HD-19-A, G52012",
      "product_quantity": "1 Unit OUS",
      "reason_for_recall": "Devices may contain elevated levels of bacterial endotoxin.",
      "recall_initiation_date": "20240401",
      "center_classification_date": "20240516",
      "report_date": "20240522",
      "code_info": "Catalogue Number: ECHO-HD-19-A; GPN: G52012; UDI/DI: 00827002520127; Lot Numbers: C2145003 and C2144407."
    }
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}