{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "52634",
      "recalling_firm": "NuVasive Inc",
      "address_1": "7475 Lusk Blvd",
      "address_2": "N/A",
      "postal_code": "92121-5707",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution-including the states of OR, MO, FL, WI, CA, and NC.",
      "recall_number": "Z-0364-2013",
      "product_description": "7.5mm x 45mm Cannulated Screw Shank    Subsequent Codes: KWP, KWQ, MNH, MNI",
      "product_quantity": "240 units total",
      "reason_for_recall": "The tulip portion of the screw assembly can disengage from the shank after implantation.",
      "recall_initiation_date": "20090105",
      "center_classification_date": "20121119",
      "termination_date": "20121119",
      "report_date": "20121128",
      "code_info": "Batch: JK2099, JK2186"
    }
  ]
}