{
  "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": "Allendale",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96349",
      "recalling_firm": "Stryker Spine",
      "address_1": "59 State Rt 17 S",
      "address_2": "",
      "postal_code": "07401-1614",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "",
      "distribution_pattern": "Domestic: CA, CO, FL, GA, IL, MA, NE, NH, NY, OK, PA, TX, UT.  International: Canada.",
      "recall_number": "Z-1490-2025",
      "product_description": "Monterey AL Implant Inserter; 18/20mm; Catalog 48019130.",
      "product_quantity": "46 units (44 US, 2 OUS)",
      "reason_for_recall": "Potential for the gold unlock button to separate from the inserter.",
      "recall_initiation_date": "20250228",
      "center_classification_date": "20250331",
      "report_date": "20250409",
      "code_info": "Catalog 48019130; UDI-DI: 07613327501049; Lot Number: 231639;",
      "more_code_info": ""
    }
  ]
}