{
  "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": "Ongoing",
      "city": "Aliso Viejo",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89177",
      "recalling_firm": "NuVasive Specialized Orthopedics, Inc.",
      "address_1": "101 Enterprise Ste 100",
      "address_2": "",
      "postal_code": "92656-2604",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide",
      "recall_number": "Z-0528-2022",
      "product_description": "MAGEC 1 System",
      "product_quantity": "3,056 devices",
      "reason_for_recall": "Safety Alert to all surgeons informing them of post-implantation fractures of an internal metallic component for device manufactured prior to March 26, 2015.",
      "recall_initiation_date": "20190625",
      "center_classification_date": "20220126",
      "report_date": "20220202",
      "code_info": "All MAGEC Systems (Serial/Lot Numbers) manufactured prior to March 26, 2015.",
      "more_code_info": ""
    }
  ]
}