{
  "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": "2026-07-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Haltom City",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99342",
      "recalling_firm": "Medtronic Neurosurgery",
      "address_1": "4620 N Beach St",
      "address_2": "N/A",
      "postal_code": "76137-3219",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of UT, AL, CA, NC, GA, AR, LA, KY, LA, KY, IL, OK and the country of Costa Rica.",
      "recall_number": "Z-2768-2026",
      "product_description": "Ventriculostomy Kit, REF: 46154",
      "product_quantity": "167",
      "reason_for_recall": "Ventriculostomy devices, used during ventriculostomy procedures to gain access to the ventricular system, may exhibit endotoxin levels that exceed the acceptable limit for devices that come into contact with cerebrospinal fluid; endotoxin exposure can cause an acute inflammatory process.",
      "recall_initiation_date": "20260617",
      "center_classification_date": "20260721",
      "report_date": "20260729",
      "code_info": "UDI-DI: 00673978947396, Lot: 2025-08779"
    }
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}