{
  "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": "Terminated",
      "city": "Allendale",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72495",
      "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": "Nationwide Distribution.",
      "recall_number": "Z-0222-2016",
      "product_description": "Stryker UniVise Spinous Process Fixation Plate System Inserter, Stryker Spine, Non-Sterile.  Reference Number 48590100. Manual Surgical Instrument.",
      "product_quantity": "41 units",
      "reason_for_recall": "The Inserter Inner Shaft would not fit through the Inserter. The inner diameter of the cannulated shaft of the inserter was undersized.",
      "recall_initiation_date": "20150908",
      "center_classification_date": "20151105",
      "termination_date": "20190114",
      "report_date": "20151111",
      "code_info": "Reference Number 48590100 Lots B40155, B34446, B34447 and B41171."
    }
  ]
}