{
  "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": {
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      "city": "Irvine",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92702",
      "recalling_firm": "Medtronic Neurosurgery",
      "address_1": "5290 California Ave",
      "address_2": "",
      "postal_code": "92617-3073",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "recall_number": "Z-2412-2023",
      "product_description": "Medtronic REF 46915 Duet External Drainage and Monitoring system, Interlink Injection sites, Ventricular Catheter, STERILE EO, Rx Only",
      "product_quantity": "44 units",
      "reason_for_recall": "Product labeling contains incorrect expiration date",
      "recall_initiation_date": "20230628",
      "center_classification_date": "20230817",
      "report_date": "20230823",
      "code_info": "Lot # 226632942; UDI-DI: 00763000624781",
      "more_code_info": ""
    }
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}