{
  "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": "93573",
      "recalling_firm": "Stryker Spine",
      "address_1": "2 Pearl Ct",
      "address_2": "N/A",
      "postal_code": "07401-1611",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: MD, MI, NM, TX & OUS: Canada & France.",
      "recall_number": "Z-0610-2024",
      "product_description": "LITe Decompression Snake Arm, REF 48080230",
      "product_quantity": "9",
      "reason_for_recall": "Product arm was manufactured with the incorrect clamp component. As a result, the affected product arm cannot attach to the arm post shaft.",
      "recall_initiation_date": "20231101",
      "center_classification_date": "20231221",
      "report_date": "20231227",
      "code_info": "UDI-DI (GTIN): 07613327263909, lot # 227764."
    }
  ]
}